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    "parties": [
      "SOUTHERN ILLINOISAN, Appellee, v. THE ILLINOIS DEPARTMENT OF PUBLIC HEALTH et al., Appellants."
    ],
    "opinions": [
      {
        "text": "JUSTICE McMORROW\ndelivered the judgment of the court, with opinion.\nChief Justice Thomas and Justices Freeman, Fitzgerald, Kilbride, Garman and Karmeier concurred in the judgment and opinion.\nOPINION\nPlaintiff, the Southern Illinoisan newspaper, requested the Illinois Department of Public Health (Department) to release from the Illinois Health and Hazardous Substances Registry (Cancer Registry) certain data about incidents of neuroblastoma, a rare form of childhood cancer. The Department denied plaintiff\u2019s request. Thereafter, plaintiff filed a complaint in the circuit court of Jackson County pursuant to the Freedom of Information Act (FOIA) (5 ILCS 140/1 et seq. (West 1998)), requesting judicial review of the Department\u2019s denial. The circuit court granted plaintiff summary judgment and ordered the Department to release the requested data. The appellate court reversed the judgment of the circuit court and remanded the cause for further proceedings. 319 Ill. App. 3d 979 (2001) (Southern Illinoisan I). After a bench trial, the circuit court of Jackson County again ordered the release of the requested information. The appellate court affirmed the judgment of the circuit court and directed the Department to release the information requested by plaintiff. 349 Ill. App. 3d 431 (Southern Illinoisan IT). For the reasons that follow, we affirm the judgment of the appellate court.\nBACKGROUND\nWe limit our discussion of the factual background and procedural history of the instant cause to only those points relevant to the issue presented in this appeal. Plaintiff, the Southern Illinoisan, is a daily newspaper published in Carbondale, Illinois. On October 28, 1997, plaintiff made a written request, pursuant to the FOIA (5 ILCS 140/3 (West 1998)), that the Department provide plaintiff with copies of documents relating to the incidence of neuroblastoma in Illinois from 1985 to the date of the request. In its request, plaintiff wrote that it believed that these documents were \u201cavailable by type of cancer, zip code and date of diagnosis,\u201d and asked that the information be delivered to plaintiff in that format. Plaintiff did not request that the Department release any other identifying information, such as the patients\u2019 names or addresses. In a letter dated November 18, 1997, the Department denied plaintiff\u2019s FOIA request. The Department based this denial on sections 7(l)(a) and (l)(b) of the FOIA (5 ILCS 140/7(l)(a), (l)(b) (West 1998)), which protects information that is specifically exempted from disclosure under state law. According to the Department, the Medical Studies Act (735 ILCS 5/8\u2014 2101 (West 1998)) prohibited the Department from disclosing any information \u201ccollected in a medical study.\u201d\nOn November 24, 1997, plaintiff appealed the denial of its FOIA request to Dr. John R. Lumpkin, the Director of the Department. In a letter dated December 4, 1997, Dr. Lumpkin reaffirmed the denial of plaintiffs FOIA request. In his letter to plaintiff, Dr. Lumpkin explained the basis for the denial: \u201cAfter reviewing the request, I must affirm the Department\u2019s denial of the information regarding the incidence of neuroblastoma by zip code and date of diagnosis based on the Medical Studies Act (735 ILCS 5/8 \u2014 2101). I believe this information is, and should continue to be, protected as it is information collected in a medical study.\u201d\nOn January 23, 1998, plaintiff filed a complaint in the circuit court of Jackson County, pursuant to section 11 of the FOIA (5 ILCS 140/11 (West 1998)). The complaint requested, inter alia, judicial review of the Department\u2019s denial of plaintiffs information request. Plaintiff contended that no statutory disclosure exemption applied to the records it had requested from the Department. According to plaintiff, the records it sought to obtain from the Department under the FOIA were clearly of significant interest to the general public, as they would \u201creveal the existence or non-existence of cancer clusters in the State of Illinois.\u201d In support of its request for disclosure, plaintiff cited to the appellate court\u2019s decision in May v. Central Illinois Public Service Co., 260 Ill. App. 3d 41 (1994), as controlling.\nOn June 8, 2005, plaintiff filed in the circuit court a motion for judgment on the pleadings or, in the alternative, a motion for partial summary judgment. According to plaintiff, the Department, in its answer to plaintiffs complaint, failed to raise any statutory exemption as an affirmative defense to plaintiff\u2019s FOIA request for disclosure. In addition, plaintiff asserted, the Department had failed to raise any factual basis in support of the claim that the documents were exempt from disclosure. Plaintiff argued that the instant cause was factually analogous to the appeal in May, wherein the appellate court upheld the trial court\u2019s order directing the Department to disclose records identical to those requested in this cause. Plaintiff noted that in May, the court held that the release of the records from the Cancer Registry by type of cancer, date of diagnosis and ZIP code would not result in an invasion of patient privacy. Accordingly; plaintiff asserted, a similar result was warranted here, and there existed no genuine issue of material fact to preclude entry of summary judgment in its favor.\nThereafter, the Department filed a response to plaintiffs summary judgment motion, as well as its own cross-motion for summary judgment. The Department argued, inter alia, that because disclosure of the information sought by plaintiff was prohibited by the Illinois Health and Hazardous Substances Registry Act (Registry Act) (410 ILCS 525/1 et seq. (West 1998)), it was therefore exempt under section 7(l)(a) of the FOIA (5 ILCS 140/ 7(1)(a) (West 1998)). The Department explained in its pleadings that it could not satisfy plaintiffs FOIA request because although the FOIA provides that \u201ceach public body shall make available to any person for inspection or copying all public records\u201d (see 5 ILCS 140/3 (a) (West 1998)), there are certain exceptions to disclosure, including \u201c[ijnformation specifically prohibited from disclosure by *** State law or rules or regulations adopted under *** State law\u201d (see 5 ILCS 140/7(l)(a) (West 1998)). The Department argued that the information requested by plaintiff was prohibited from disclosure under this provision because the Registry Act precludes disclosure of information which reveals \u201c[t]he identity, or any group of facts which tends to lead to the identity, of any person whose condition or treatment is submitted to the Illinois Health and Hazardous Substances Registry.\u201d See 410 ILCS 525/4(d) (West 1998).\nIn support of its position, the Department attached the affidavit of Dr. Latanya Sweeney, Ph.D., a professor of computer science and public policy at Carnegie Mellon University. In her affidavit, Dr. Sweeney attested that, at the behest of the Department, she conducted an experiment to determine if persons listed in the Cancer Registry could be identified from only the three information fields requested by plaintiff: the type of cancer, the date of diagnosis, and the patient\u2019s ZIP code. According to Dr. Sweeney, she compared the data in these three information fields to other data sets that are available to the general public, such as patient names, addresses, phone numbers, financial information, and other medical information. Even though the data in the Cancer Registry did not have identifiers such as names, addresses and telephone numbers, Dr. Sweeney attested that through her experiment she could \u201cshow how persons can be re-identified from the Illinois Cancer Registry when the combination of data elements that includes only type of cancer, date of diagnosis, and zip code is provided.\u201d According to Dr. Sweeney, her experiment \u201cestablished] that a significant number of individuals in the general public with access to a personal computer, using traditional database software, who purchase or acquire public data sets will be able to reidentify individuals in the Illinois Cancer Registry,\u201d as this \u201cseemingly anonymous information can be re-identified by linking the information to databases that are made available to the public.\u201d\nFinally, although the Department noted that plaintiff relied upon the May case, and also acknowledged that in May the court was faced with the same issue as in the instant matter, the Department attempted to draw one crucial difference between May and the instant cause: the court in May was not presented with any definitive showing of how the data contained in the Cancer Registry could be reidentified. The Department asserted that, based upon Dr. Sweeney\u2019s affidavit, it established how the dissemination of this information could tend to lead to a patient\u2019s identity, and, therefore, that the disclosure of the information was prohibited.\nOn December 31, 1998, the circuit court granted plaintiffs motion for summary judgment, and denied the Department\u2019s cross-motion for summary judgment. In the course of its ruling, the court noted that it had made an in camera inspection of the records requested by plaintiff under the FOIA and determined that the appellate court\u2019s decision in May was controlling. Accordingly, in its order, the circuit court directed the Department to \u201cproduce the Illinois Cancer Registry by listing the type of cancer, date of diagnosis and zip code of each cancer patient from 1985 to present.\u201d The circuit court also ordered that the parties were \u201crestricted from identifying or attempting to identify or contact cancer patients from information produced pursuant to this action.\u201d On July 22, 1999, the circuit court denied the Department\u2019s motion for reconsideration.\nOn appeal, the appellate court reversed the circuit court\u2019s grant of summary judgment to plaintiff. 319 Ill. App. 3d 979 (2001) (Southern Illinoisan I). Relevant to the instant appeal, the Department had argued, inter alia, that the disclosure exemption in section 7(1) (a) of the FOIA (5 ILCS 140/7(1)(a) (West 1998)), which exempts from release information specifically prohibited from disclosure by federal or state law, precluded the release of the information requested by plaintiff. The Department asserted that disclosure of the information requested by plaintiff would violate section 4(d) of the Registry Act (410 ILCS 525/4(d) (West 1998)), which provides that the \u201cidentity, or any group of facts that tends to lead to the identity, of any person whose condition or treatment is submitted\u201d to the Cancer Registry is confidential and not open to public inspection or dissemination. The appellate court agreed with the Department that there was a genuine issue of material fact as to this issue.\nAlthough plaintiff argued that Dr. Sweeney\u2019s affidavit was conclusory, the appellate court disagreed. The appellate court held that Dr. Sweeney\u2019s affidavit raised a genuine issue of material fact, namely: \u201cIs the requested data that which tends to lead to the identity of any person whose condition is submitted to the Department?\u201d 319 Ill. App. 3d at 986. The appellate court held that in answering this question, the circuit court was to read in a \u201creasonableness\u201d requirement in determining whether the requested information constituted a \u201cgroup of facts which tends to lead to the identity\u201d of cancer patients, within the meaning of section 4(d) of the Registry Act. The appellate court explained its reasoning as follows:\n\u201cThe phrase \u2018group of facts that tends to lead to the identity\u2019 must mean any group of facts that reasonably would tend to lead to the identity of specific persons. The entire purpose of the Cancer Registry Act (see 410 ILCS 525/2(h), (c) (West 1998)) would be effectively repealed by subsection 4(d) if we did not impose the reasonableness requirement, because any fact, no matter how unrelated to identity can tend to lead to identity, and, therefore, any and every fact would be exempt under subsection 4(d). However, since one purpose of the Cancer Registry Act is to provide information to the public, this cannot be what the legislature intended. If, however, one reads the statutory phrase as precluding the release of information that reasonably would tend to lead to identity, some information is exempt, while other information is not exempt. In our judgment, whether the information sought in this case would reasonably tend to lead to the identity of particular individuals presents a question of fact.\u201d (Emphases in original.) 319 Ill. App. 3d at 987.\nBecause the appellate court found that a genuine issue of material fact was presented, it therefore held that the trial court erred in entering summary judgment in favor of plaintiff. Accordingly, the appellate court remanded this cause to the trial court for further proceedings. 319 Ill. App. 3d at 987.\nUpon remand, the circuit court held a bench trial on June 6, 2002. Because the FOIA places the burden of proof upon the public body to establish that its refusal of disclosure is in accordance with the FOIA (5 ILCS 140/ 11(f) (West 1998)), the Department put on its case first. The Department\u2019s first witness was Janice Snodgrass, the manager of the Cancer Registry. She testified that the Cancer Registry is a \u201ccancer database surveillance system,\u201d meaning that it contains information that has been reported to the Department pursuant to the Registry Act from approximately 400 different reporting sources. The Registry Act requires mandated reporting of cancer cases from all Illinois hospitals, as well as from ambulatory surgical centers and freestanding radiation treatment centers. In addition, there is voluntary reporting by some physicians, dermatologists, and pathology labs. Also, Snodgrass testified, there is data exchange from 13 other states where Illinois patients might have migrated.\nSnodgrass testified that the Cancer Registry is maintained on a computer, and the information in the Registry consists of demographic information that identifies the patient, including his or her address, the patient\u2019s county of residence, the patient\u2019s race and gender, and whether the patient used alcohol and/or tobacco. The Cancer Registry also contains patient medical information, including the patient\u2019s type of cancer, how it was diagnosed, the date of diagnosis, how much it has spread, and treatment and survival information.\nSnodgrass testified that although the very specific information contained within the Cancer Registry \u2014 such as patient identity and residence \u2014 is kept strictly confidential, a public data set from the Cancer Registry is available on the Department\u2019s Web site. This public data set contains very limited information, and provides this information at the state, county and ZIP code levels. According to Snodgrass, as the geographical areas become smaller, less information is available to protect patient confidentiality. Although the Department provides public data sets of information from the Cancer Registry, Snodgrass testified that plaintiffs request for information was problematic because plaintiff asked that the Department disclose the specific number of neuroblastoma cases, along with date of diagnosis and the patient\u2019s ZIP code. According to Snodgrass, the public data sets do not specifically disclose whether a certain case is a neuroblastoma case. Snodgrass testified that if an individual wishes to obtain information beyond that which is available in the public data set, the Registry Act provides that the requestor must fill out an application for access to the data, as well as sign a confidentiality agreement. The application is then processed by an internal review board, which then determines whether disclosure will be made. According to Snodgrass, plaintiff did not avail itself of this procedure.\nOn cross-examination, Snodgrass was asked if she was aware of recent occurrences of claims of neuroblastoma caused by site-specific environmental causes. She responded \u201cyes\u201d to this question. Snodgrass testified, however, that the raw data is not information which is available to the public. A scientist or researcher, however, could request this information from the Department if the purpose for the request was to perform an investigation.\nThe Department\u2019s second \u2014 and final \u2014 witness at trial was Dr. Latanya Sweeney. Dr. Sweeney testified that she is an assistant professor of computer science and public policy at Carnegie Mellon University, and also the University\u2019s director of the Laboratory for International Data Privacy. Dr. Sweeney joined Carnegie Mellon in 1998, and, prior to that, she worked as an instructor at Harvard University. Dr. Sweeney stated that she has an undergraduate degree in computer science from Harvard University, a master\u2019s degree in computer science and electrical engineering from MIT, and a Ph.D. in computer science from MIT. Dr. Sweeney testified that she has served as an expert witness in numerous cases involving data privacy questions and the anonymity of data, and that she has worked as a consultant for several governmental agencies. Based upon her credentials, the circuit court qualified Dr. Sweeney as an expert witness on the subject of data anonymity.\nDr. Sweeney testified that she was contacted by the Department in 1998, and asked whether she could reidentify individuals contained in the Cancer Registry based upon the Registry information and anything else she could find from other public sources. The data fields she was given from the registry were the type of cancer, the date of the diagnosis and the ZIP code in which the patient resided \u2014 the identical fields of information requested by plaintiff in its FOIA request. Dr. Sweeney testified that in conducting this experiment she used a regular laptop computer, commercially available spreadsheet software, the information from the Cancer Registry sought by plaintiff, and any other information that she could obtain through Internet access. Upon completion of her experiment, Dr. Sweeney testified, she was able to supply a single correct name for 18 of 20 sets of data given to her by the Department from the Cancer Registry. In addition, Dr. Sweeney was able to suggest two alternative names \u2014 one of which was correct \u2014 for the remaining two data sets. According to Dr. Sweeney, the information in the Cancer Registry requested by plaintiff \u2014 the date of diagnosis, patient\u2019s ZIP code and type of cancer\u2014 could be correctly reidentified in from 80% to 87% of all instances.\nDr. Sweeney then went on to testify at length as to the exact steps that she took in order to arrive at these identifications. The circuit court, fearing that Dr. Sweeney\u2019s testimony could serve as an \u201cinstruction book\u201d for anyone attempting to replicate what Dr. Sweeney had done, sealed that portion of Dr. Sweeney\u2019s testimony in which she set forth the methodology she used to make these identifications. We have thoroughly examined Dr. Sweeney\u2019s sealed testimony for the purposes of this appeal. Without divulging the specifics of the testimony placed under seal by the circuit court, we briefly outline, in general terms, the method employed by Dr. Sweeney in her experiment.\nDr. Sweeney testified that she used a multistep method to identify the individuals in the Cancer Registry. She stated that she began by researching the disease of neuroblastoma to familiarize herself with its symptoms, diagnosis and treatment. She then purchased several publicly available data sets, ranging in price from a few hundred dollars to over a thousand dollars. Dr. Sweeney testified that her costs associated with this experiment were approximately $2,000. Dr. Sweeney stated that she used some \u201csemi-public\u201d data sets, which she described as a \u201cslightly more expensive version\u201d of the public data set which contains the same information but in an easier-to-examine format. Dr. Sweeney testified that, in most instances, in order to obtain the information she used in her experiment, she had to fill out forms, wait for her request to be processed, and received the records in the mail in a CD format.\nBased upon what she learned through her research on neuroblastoma, Dr. Sweeney \u2014 with the assistance of a spreadsheet computer program \u2014 then searched the public data sets for what she believed would be relevant information leading to the identification of patients afflicted with this specific disease. Dr. Sweeney commented that some of the data sets she used consisted of files which contained \u201cabout a million records.\u201d She stated that she scrutinized the data sets to determine what factors neuroblastoma cases may have in common. At one point, Dr. Sweeney testified, she settled on a certain factor. However, when she used that factor as part of her analysis, she discovered that she had .made a mistake, as that particular factor was far too broad and, accordingly, encompassed far too many cases other than those of neuroblastoma. Dr. Sweeney then went back to the data sets and focused on a second factor which she believed was common to all neuroblastoma cases. This time, Dr. Sweeney testified, when she ran this particular factor through her analysis, she had discovered that she had found a far more accurate match. She then gathered information from other on-line sources, as well as from libraries and newspaper archives, in order to accurately arrive at the names of 18 of 20 individuals listed in the Registry.\nDr. Sweeney stated that she was able to make these identifications almost solely by use of the information she discovered in the publicly available data sets. According to Dr. Sweeney, the use of the data that she received from the Cancer Registry performed two functions. First, the Cancer Registry information helped to narrow the fields of the ZIP codes that she used in her search of the public records. Second, she was able to check the accuracy of her analysis by using the Registry information to verify that the individuals that she believed were afflicted with neuroblastoma actually had that disease.\nWhen asked whether she could identify neuroblastoma patients from the publicly available data sets without resorting to the information in the Cancer Registry, Dr. Sweeney responded, \u201cYes, I can definitely identify neuroblastoma patients, but would I be accurate or would I be correct or accurate is a different question ***.\u201d In her testimony, Dr. Sweeney characterized the Cancer Registry as the \u201cgold standard\u201d that allowed her to match the results she obtained from the public data sets for accuracy, and also informed her how good the profile of the neuroblastoma victim that she created was. Dr. Sweeney stated that although she could identify the neuroblastoma patients without the information contained in the Cancer Registry, only relying upon the publicly available data sets, she also stated that she \u201ccould not do it with that method with confidence, not with this kind of accuracy.\u201d\nDr. Sweeney concluded her testimony by stating that, in her opinion, it is very easy for anyone to identify persons from the Cancer Registry using public data sets. She explained:\n\u201cIt is very easy in the following sense, all I used was commonly available PC technology *** [and] readily available software *** and all that was required were the simple programs of using [spreadsheets]. *** They come almost on every machine now days *** so they don\u2019t require you have any programming or require you to take a computer class, but they do require you to know the basics of how to use the machine and how to use those simple packages.\u201d\nUpon the conclusion of Dr. Sweeney\u2019s testimony, the Department rested its case. Plaintiff presented no witnesses.\nThe circuit court, in an oral ruling, delivered its judgment immediately after the parties concluded closing arguments. The circuit court focused on the issue as framed by the appellate court: whether the information sought by plaintiff reasonably tended to lead to the identity of any person whose condition or treatment is submitted to the Cancer Registry, thereby violating section 4(d) of the Registry Act, and in turn, making the information exempt under section 7(l)(a) of the POIA. The court answered this question in the negative, and explained its reasoning as follows:\n\u201cI have to make a determination of what reasonable is, and to say that with the three factors that are requested by plaintiff, a reasonable person could walk to a computer and get this \u2014 use this information to determine what children in a given community have neuroblastoma, I don\u2019t think is correct. They don\u2019t have the computer skills. They don\u2019t have the knowledge of information databases, I think don\u2019t have the knowledge as to how to do \u2014 or the analytical skills is what I am trying to say. *** [H]ow many people have the thousands of dollars and we\u2019ll even say hundreds of dollars necessary to secure the databases to get this done? The key has to be that the information requested reasonably tends to lead to the identity of specific persons. It does not lead in this case. It affirms or confirms information which is gathered from other databases. *** Taking the [Cancer Registry] information in and of itself divorced from this other information *** leads nowhere.\nSo, it is the finding of the court that the information requested will not reasonably tend to lead to the identification of individuals. The right of the public to the information requested is best met by disclosure due to the substantial health risk of the condition for which the information is sought. The court orders that the information requested be provided and that the plaintiff directly or indirectly shall not attempt to locate any individuals who may be an individual contained in the statistics released.\u201d\nOn June 7, 2002, the circuit court entered a written order of judgment, memorializing the oral ruling it rendered on the previous day. In holding that the information requested by plaintiff did not \u201creasonably tend to lead to the identity of specific persons,\u201d the court provided additional reasoning in support of its result:\n\u201cThe knowledge which Dr. Sweeney acquired during her education and in her professional career provided her with a foundation upon which she drew in conducting her experiments. This knowledge allowed her to know which data bases to look for and to cross index. The foundation of knowledge acquired by Dr. Sweeney is unique but not exclusive. It is not reasonable to believe that someone with less knowledge, education and experience in this area would be as successful as Dr. Sweeney in using the information to arrive at the same result she achieved.\nIt was the unique data bases of information which were utilized by Dr. Sweeney that provided the identifying information rather than the information which was requested by the plaintiff. Even without the information requested by the plaintiff, Dr. Sweeney testified she would be able to identify specific individuals.\nThe information requested by the plaintiff does not lead to the identification of individuals. The information requested may confirm results of analysis of data retrieved from other sources. However, the information, in and of itself, does not lead to the identification. It is one *** piece of information in a melange of data which, when properly analyzed, could assist in confirming the identity of individuals. This falls far short of \u2018reasonably tending to lead to the identity of particular individuals.\u2019 \u201d\nOn appeal, the appellate court affirmed the circuit court\u2019s judgment directing the Department to release the data requested by plaintiff. 349 Ill. App. 3d 431 (Southern Illinoisan II). The appellate court rejected the Department\u2019s assertion that an individual did not need to be a professor from MIT to discover the identity of Cancer Registry members from the data plaintiff requested in this case. \u201cAlthough it is true, as the defendants contend, that Dr. Sweeney testified that she did her work on a simple laptop computer using standard, readily available software, we do not believe that it was Dr. Sweeney\u2019s equipment alone or her equipment in conjunction with a passing knowledge of computing that made it possible for her to identify the subjects in question. Rather, it was, as the circuit court noted, her knowledge, education, and experience that allowed her to make the identifications.\u201d Southern Illinoisan II, 349 Ill. App. 3d at 434.\nAccordingly, the appellate court found it difficult to believe that an average person with less knowledge, education and experience than Dr. Sweeney would have been able to construct and navigate the multistep methodology used to identify those listed as part of the Cancer Registry. In addition, the appellate court found that Dr. Sweeney\u2019s testimony failed to present the court with a reasoned measure of the threat that might exist from the release of this information to plaintiff or, for that matter, to the public in general. The appellate court explained:\n\u201c[W]hile the evidence presented by the defendants demonstrates that one expert in data anonymity was able to identify the subjects in question from the data requested by the plaintiff, following her own six-step process and drawing upon her years of education, knowledge, and experience to analyze the data to the extent necessary to identify the subjects in question, that evidence does not concretely and conclusively demonstrate that a threat exists that other individuals, even those with skills approaching those of Dr. Sweeney, likewise would be able to identify the subjects or what the magnitude of such a threat would be, if it existed. Are there two people in the entire State of Illinois who could replicate Dr. Sweeney\u2019s results with the same limited data or are there two thousand? Are there zero or are there a million? These questions are significant because without some sense of the magnitude of the alleged threat of which the defendants complain, it is very difficult for this court to determine whether the data in question reasonably tends to lead to the identity of specific persons.\u201d Southern Illinoisan II, 349 Ill. App. 3d at 435. The appellate court noted that, in its prior opinion in\nSouthern Illinoisan I, it held that it is necessary to impose a \u201creasonableness\u201d requirement in assessing whether the information requested by plaintiff from the Cancer Registry consists of a \u201cgroup of facts that tends to lead to the identity\u201d of those listed in the Registry. Applying that rule to the facts presented, the appellate court held that the Department did not meet this burden. The appellate court explained:\n\u201c[T]he fact that one expert in data anonymity can manipulate data to determine identify does not necessarily mean, without more, that a threat exists that other individuals will be able to do so as well, nor does it in any way define the magnitude of such a threat or whether that threat, if it in fact even exists, renders the release of the data an act that reasonably tends to lead to the identity of specific persons. To find otherwise would undermine the reasonableness requirement and would effectively remove it from our analysis, leading to a situation where if it could be shown that one expert could identify individuals from information released, then the release of that information would automatically be deemed to reasonably tend to lead to the identity of specific persons.\u201d Southern Illinoisan II, 349 Ill. App. 3d at 436.\nThis court granted the Department\u2019s petition for leave to appeal pursuant to our Rule 315 (177 Ill. 2d R. 315). We also granted leave to the Associated Press, the Copley Press, Inc., Gannett Company, Inc., the Illinois Press Association and the Tribune Company to file an amicus curiae brief in support of plaintiff.\nANALYSIS\nThis appeal presents the sole question of whether the information requested from the Department by plaintiff pursuant to the FOIA \u201ctends to lead to the identity\u201d of patients listed in the Cancer Registry, thereby violating section 4(d) of the Registry Act (410 ILCS 525/4(d) (West 1998)). If so, then the information requested by plaintiff is exempt from disclosure under section 7(l)(a) of the FOIA (5 ILCS 140/7(l)(a) (West 1998)).\nThe Department contends that the appellate court erred in affirming the circuit court\u2019s order that the Department disclose the Cancer Registry information requested by plaintiff. The Department begins its argument by observing that when a citizen of this state is diagnosed with cancer, that fact is mandatorily reported to the Department and the patient\u2019s information is recorded in the Cancer Registry. The Department notes that the collection of such health information implicates the privacy concerns of the patients whose information is contained within the Registry. The Department asserts that the subsequent dissemination of the collected health information multiplies the potential privacy loss, especially if that dissemination is to a newspaper, such as plaintiff. Accordingly, the Department maintains, the legislature sought to restrict the dissemination of the patient information contained within the Cancer Registry. To this end, the Department asserts, the legislature prohibited within section 4(d) of the Registry Act the disclosure not only of the identity of the patient, but also of any information or group of information that even \u201ctends to lead\u201d to the identity of any person whose condition or treatment is submitted to the Registry.\nThe Department contends that the lower courts applied an incorrect legal standard in this case, one that is at odds with the standard established by the General Assembly. According to the Department, the lower courts departed from the well-settled rule that in construing a statute, the plain language of the enactment must be used. The Department maintains that the appellate court erred in reasoning that all information in some remote fashion would \u201ctend to lead to the identity\u201d of cancer patients, and therefore incorrectly advised the circuit court to determine whether the release of the information would reasonably tend to lead to the identity of specific persons. Although the Department acknowledges in its brief to this court that the word \u201ctends\u201d is \u201cadmittedly not very precise and potentially might be interpreted too broadly,\u201d the Department also takes the position that the legislature used the word \u201ctends\u201d to indicate a broader prohibition than just information that simply \u201cleads to the identity\u201d of cancer patients. According to the Department, the appellate court\u2019s addition of the word \u201creasonably\u201d to the \u201ctends to lead to the identity\u201d standard does not improve the analysis. The Department asserts that the word \u201creasonably\u201d has the same imprecise quality as the word \u201ctends,\u201d and it can be \u201cinterpreted so broadly that it nullifies the word \u2018tends\u2019 and thwarts the legislative purpose in using that word.\u201d\nThe Department also argues that the uncontested evidence presented in the cause before us demonstrates that the Cancer Registry information requested by plaintiff tends to lead to the identity of cancer patients. The evidence includes Dr. Sweeney\u2019s unrebutted assertion that 80% to 87% of the individuals in the Cancer Registry could be uniquely and correctly identified if the Department released the data requested by plaintiff. The record also includes Dr. Sweeney\u2019s expert opinion that a number of individuals in the general public with access to a personal computer, using traditional database software, who purchase or acquire public data sets, will be able to identify individuals listed in the Cancer Registry. Thus, the Department argues, the record establishes that the three data elements requested by plaintiff \u2014 the patient\u2019s type of cancer, the date of diagnosis and the patient\u2019s ZIP code \u2014 tend to lead to the identity of cancer patients and therefore violates section 4(d) of the Registry Act.\nIn addition, the Department asserts that the appellate court in Southern Illinoisan II \u201csignificantly exaggerate[d] [the] complexity\u201d of Dr. Sweeney\u2019s experiment. The Department also states that even though Dr. Sweeney testified that the Cancer Registry information only assisted her in confirming the identity of the individuals, this testimony is sufficient to establish that the information requested by plaintiff under the FOIA \u201ctends to lead\u201d to the identities of the patients listed in the Registry.\nWith respect to the appellate court\u2019s prior decision in May, the Department asserts that Dr. Sweeney\u2019s testimony is a crucial distinguishing factor between that case and the instant matter. The Department asserts that the May court\u2019s observation that it could not see how dissemination of a person\u2019s ZIP code, type of cancer and date of diagnosis could tend to lead to the patient\u2019s identity describes a situation that is directly contrary to the factual evidence presented in the instant case as a result of Dr. Sweeney\u2019s testimony.\nFinally, the Department also criticizes the lower courts for stressing only one of the purposes of the Cancer Registry \u2014 to provide information to the public\u2014 and connecting that purpose to the release of raw public data. The Department asserts that the courts overlooked that the Registry Act has not one, but several, goals, and that releasing raw data is neither the only \u2014 nor the best \u2014 way to achieve the Act\u2019s purposes.\nFor all of the above reasons, the Department concludes that the information requested by plaintiff from the Cancer Registry tends to lead to the identity of cancer patients included in the Registry. Accordingly, the Department asserts, the information is prohibited from disclosure under section 4(d) of the Registry Act and, therefore, exempt from disclosure under section 7(l)(a) of the FOIA (5 ILCS 140/7(l)(a) (West 1998)).\nIn response, plaintiff asserts that the appellate court correctly affirmed the judgment of the circuit court requiring the Department to comply with plaintiffs FOIA request. Plaintiff contends that the FOIA is to be interpreted in favor of disclosure and that the exemptions from disclosure are to be read narrowly. In addition, plaintiff asserts, the public policy concerns which underpin the Registry Act \u2014 most specifically that the Registry information be used to alert citizens about risks, early detection and treatment of cancers known to be elevated in their communities \u2014 favor disclosure of the information requested by plaintiff. Although plaintiff acknowledges that the Registry Act has an \u201cinherent tension\u201d between patient privacy and a community\u2019s right to know about elevated levels of cancer in its geographic area, plaintiff argues that the balance is tipped by the fact that the FOIA is to be given a liberal interpretation and that the exceptions to disclosure are narrow.\nIn addition, plaintiff contends, the lower courts correctly ruled that the Department did not meet its burden of proof in this case. Plaintiff emphasizes that under the FOIA, the Department bears the burden of proof to establish that an exemption from disclosure applies. According to plaintiff, a review of the record reveals that at no point did the Department demonstrate that release of the requested information would tend to lead to the identity of any person whose condition or treatment was submitted to the Cancer Registry.\nWith respect to Dr. Sweeney\u2019s experiment, plaintiff stresses that Dr. Sweeney is an expert at adeptly working with all types of data, and that she possesses knowledge through her education and career which allowed her to easily perform the experiment. Plaintiff asserts that, based upon Dr. Sweeney\u2019s testimony, it was apparent that she knew which data sets to use, how and where to obtain these data sets, and the most efficient manner in which to review the applicable records. Plaintiff also stresses that Dr. Sweeney testified that she used public data sets \u2014 and not the Cancer Registry information \u2014 to identify individual patients. Plaintiff notes that Dr. Sweeney testified that she used the Cancer Registry information only to verify her work. In its brief to this court, plaintiff asserts that \u201c[i]f this court adopts the privacy position asserted by the Department (that privacy is invaded by the release of data by diagnosis, date of diagnosis and zip code) then it would be impossible to meet the other goals of [the Registry] Act,\u201d meaning that it will be impossible to inform health professionals and citizens of risks of cancer known to be elevated in their communities.\nPlaintiff concludes its argument by noting that in May, the appellate court had occasion to examine section 4 of the Registry Act in relation to the release of Cancer Registry neuroblastoma information identical to that requested in this case. In May, the appellate court held that the disclosure of the information was not prohibited. Plaintiff urges a similar outcome here. Plaintiff also notes that if disclosure of the information is ordered, it has agreed to be bound by the circuit court\u2019s order that it would not use the Cancer Registry information in any way to identify the individuals. In conclusion, plaintiff urges this court to affirm the rulings of the lower courts directing the Department to comply with plaintiffs FOIA request.\nIn support of the position taken by plaintiff in the instant cause, the Associated Press, the Copley Press, Inc., Gannett Company, Inc., the Illinois Press Association and the Tribune Company have filed a brief with this court as amici curiae. According to the amici news organizations, because they \u201cdepend on FOIA to open government files to public scrutiny, they have a keen interest in both the outcome of this case and its impact on the future of FOIA.\u201d The amid argue that both the language and purpose of the FOIA instruct that public records cannot be withheld unless the government meets its burden of proving, by a preponderance of the evidence, that an invasion of privacy will occur if the records are released. The amici emphasize that plaintiff is not seeking to expose private information about specific individuals. Rather, plaintiff has requested \u201cmasked\u201d data that may shed light on possible links between hazardous substances and cancer, an issue of great public interest and one that the legislature specifically contemplated in requiring the data collection under the Registry Act. The amici assert that if the data were to show that an unusual type of cancer occurred in an extraordinary number of cases in one particular ZIP code, surely that would be of concern to everyone in that ZIP code \u2014 and to people in other areas as well. The amici argue that the lower courts correctly decided that plaintiff\u2019s FOIA request should be granted, and that the requested information does not tend to lead to the identity of any patients listed in the Cancer Registry.\nIn the instant appeal, our inquiry is whether the circuit court properly granted plaintiffs FOIA request for disclosure of Cancer Registry information relating to incidences of neuroblastoma by type of cancer, the date of diagnosis and the patient\u2019s ZIP code. We reject the arguments advanced by the Department, and agree with plaintiff that the lower courts correctly required disclosure of the requested information. Our analysis begins by examining the relationship between the FOIA and the Registry Act.\nOur review of the FOIA and the Registry Act is guided by several well-established principles of statutory construction. It is well settled that the primary objective of this court when construing the meaning of a statute is to ascertain and give effect to the intent of the General Assembly. People ex rel. Sherman v. Cryns, 203 Ill. 2d 264, 279 (2003). In determining legislative intent, our inquiry begins with the plain language of the statute, which is the most reliable indication of the legislature\u2019s objectives in enacting a particular law. In re Madison H., 215 Ill. 2d 364, 372 (2005). A fundamental principle of statutory construction is to view all provisions of a statutory enactment as a whole. Accordingly, words and phrases should not be construed in isolation, but must be interpreted in light of other relevant provisions of the statute. Michigan Avenue National Bank v. County of Cook, 191 Ill. 2d 493, 504 (2000). In construing a statute, we presume that the legislature, in its enactment of legislation, did not intend absurdity, inconvenience or injustice. Burger v. Lutheran General Hospital, 198 Ill. 2d 21, 40 (2001).\nThe \u201cpurpose of the FOIA is to open governmental records to the light of public scrutiny.\u201d Bowie v. Evanston Community Consolidated School District No. 65, 128 Ill. 2d 373, 378 (1989). Accordingly, under the FOIA, \u201cpublic records are presumed to be open and accessible.\u201d Lieber v. Board of Trustees of Southern Illinois University, 176 Ill. 2d 401, 407 (1997); see also Illinois Education Ass\u2019n v. Illinois State Board of Education, 204 Ill. 2d 456, 462-63 (2003). This legislative intent is set forth by the General Assembly in section 1 of the FOIA:\n\u201cPursuant to the fundamental philosophy of the American constitutional form of government, it is declared to be the public policy of the State of Illinois that all persons are entitled to full and complete information regarding the affairs of government and the official acts and policies of those who represent them as public officials and public employees consistent with the terms of this Act. Such access is necessary to enable the people to fulfill their duties of discussing public issues fully and freely, making informed political judgments, and monitoring government to ensure that it is being conducted in the public interest.\nThis Act is not intended to be used to violate individual privacy, *** or to disrupt the duly-undertaken work of any public body independent of the fulfillment of any of the forementioned rights of the people to access to information.\nThese restraints on information access should be seen as limited exceptions to the general rule that the people have a right to know the decisions, policies, procedures, rules, standards, and other aspects of government activity that affect the conduct of government and the lives of any or all of the people. The provisions of this Act shall he construed to this end.\u201d 5 ILCS 140/1 (West 1998).\nBased upon the legislature\u2019s clear expression of public policy and intent set forth in section 1 of the FOIA that the purpose of that Act is to provide the public with easy access to government information, this court has held that the FOIA is to be accorded \u201cliberal construction to achieve this goal.\u201d Bowie, 128 Ill. 2d at 378. Accordingly, we have, on several occasions, held that the exceptions to disclosure set forth in the FOIA are to be read narrowly so as not to defeat the FOIA\u2019s intended purpose. See, e.g., Illinois Education Ass\u2019n, 204 Ill. 2d at 463; Lieber, 176 Ill. 2d at 407; American Federation of State, County & Municipal Employees (AFSCME) v. County of Cook, 136 Ill. 2d 334, 341 (1990). Therefore, \u201cwhen a public body receives a proper request for information, it must comply with that request unless one of the narrow statutory exemptions set forth in section 7 of the Act applies.\u201d Illinois Education Ass\u2019n, 204 Ill. 2d at 463; Lieber, 176 Ill. 2d at 408; AFSCME, 136 Ill. 2d at 341; 5 ILCS 140/ 3(a) (West 1998) (\u201cEach public body shall make available to any person for inspection or copying all public records, except as otherwise provided in Section 7 of this Act\u201d).\nSection 7 of the FOIA (5 ILCS 140/7 (West 1998)) sets forth a number of exemptions from disclosure, most of which are specific and identify the particular records that are shielded from disclosure. In the instant cause, the Department relies upon the exemption set forth in section 7(l)(a), which provides:\n\u201c(1) The following shall he exempt from inspection and copying:\n(a) Information specifically prohibited from disclosure by federal or State law or rules and regulations adopted under federal or State law.\u201d 5 ILCS 140/ 7(1)(a) (West 1998)).\nThis court has held that \u201c \u00a3[i]f the public body seeks to invoke one of the exemptions in section 7 as grounds for refusing disclosure, it is required to give written notice specifying the particular exemption claimed to authorize the denial.\u2019 \u201d Illinois Education Ass\u2019n, 204 Ill. 2d at 464, quoting Lieber, 176 Ill. 2d at 408; 5 ILCS 140/ 9(b) (West 1998). Any person denied his or her request for disclosure under the FOIA may appeal the denial by sending a written notice of appeal to the head of the public body. An individual has exhausted his or her administrative remedies with respect to the FOIA request if the head of the public body affirms the denial or fails to act within specified time limits. 5 ILCS 140/10 (West 1998).\nThereafter, the party seeking disclosure of the requested information may challenge the denial in the circuit court. 5 ILCS 140/ll(a) (West 1998). Section 11(f) of the FOIA (5 ILCS 140/ll(f) (West 1998)) sets forth the procedures to be followed by the circuit court in reviewing a denial of a FOIA request. This section provides that the court shall conduct the hearing \u201cde novo\u201d and shall conduct such in camera examination of the requested records as it finds appropriate to determine if such records or any part thereof may be withheld under any provision of the FOIA (5 ILCS 140/ll(f) (West 1998)). The burden shall be on the public body to establish that its refusal to permit public inspection or copying is in accordance with the provisions of the FOIA and that the records fall within the exemption it has claimed. 5 ILCS 140/ll(f) (West 1998); see also Illinois Education Ass\u2019n, 204 Ill. 2d at 464; Lieber, 176 Ill. 2d at 407-08.\nApplying this statutory framework to the matter before us, the Department bears the burden of establishing that the Cancer Registry records requested by plaintiff fall within the exemption contained in section 7(l)(a) of the FOIA: that the information is \u201cspecifically prohibited from disclosure by *** State law.\u201d 5 ILCS 140/ 7(1) (a) (West 1998). The Department asserts that the disclosure of the requested information violates section 4(d) of the Registry Act because it \u201ctends to lead to the identity, of any person whose condition or treatment is submitted to the Illinois Health and Hazardous Substances Registry.\u201d 410 ILCS 525/4(d) (West 1998). Accordingly, we turn to an examination of the Registry Act.\nIn section 2 of the Registry Act, the General Assembly set forth its legislative findings. The General Assembly stated that a serious threat to public health and welfare is posed by hazardous substances, and that\u2014 prior to the enactment of this legislation \u2014 there existed no coordinated effort to collect and analyze information with respect to hazardous substances and their potential health effects. 410 ILCS 525/2(a)(i), (a)(ii) (West 1998). In addition, the legislature acknowledged that this \u201clack of comprehensive information has caused concern on the part of Illinois citizens and a lack of effective control by the State government.\u201d 410 ILCS 525/2(a)(iii) (West 1998).\nIn response to these concerns, the General Assembly enacted the Registry Act, because \u201cit is the obligation of the State government to inform and protect the citizens of Illinois by developing a comprehensive and integrated data system on hazardous substances and public health.\u201d 410 ILCS 525/2(a)(iv) (West 1998). In sections 2(b) and (c), the legislature enumerated the purposes of the Registry Act:\n\u201c(b) It is the purpose of this Act to establish a unified Statewide project to collect, compile and correlate information on public health and hazardous substances. Such information is to be used to assist in the determination of public pohcy and to provide a source of information for the public, except when public disclosure of the information would violate the provisions of subsection (d) of Section 4 concerning confidentiality.\n(c) In particular, the purpose of the cohection of cancer incidence information is to:\n(1) monitor incidence trends of cancer to detect potential public health problems, predict risks and assist in investigating cancer clusters;\n(2) more accurately target intervention resources for communities and patients and their families;\n(3) inform health professionals and citizens about risks, early detection and treatment of cancers known to be elevated in their communities; and\n(4) promote high quality research to provide better information for cancer control and to address public concerns and questions about cancer.\u201d 410 ILCS 525/2(b), (c) (West 1998).\nAlthough it is apparent from the above-quoted sections of the Registry Act that the legislature intended the FOIA to facilitate public access to information with respect to hazardous substances and increased incidences of cancer, it is also apparent from section 4(d) of the Registry Act that, in certain instances, the General Assembly intended to limit public access to information in order to protect the privacy of cancer patients included in the Registry. At the time plaintiff made its FOIA request to the Department, section 4(d) of the Registry Act provided in pertinent part:\n\u201cThe identity, or any group of facts that tends to lead to the identity, of any person whose condition or treatment is submitted to the Illinois Health and Hazardous Substances Registry is confidential and shall not be open to public inspection or dissemination.\u201d 410 ILCS 525/4(d) (West 1998).\nSubsequently, the legislature amended section 4(d) to include a new sentence immediately following the portion quoted above:\n\u201cFacts that tend to lead to the identity of a person include the following: name, social security number, address, and any other data element that, by itself or in combination with one or more other data elements, tends to identify any person.\u201d 410 ILCS 525/4(d) (West 1998) (as amended by Pub. Act 90 \u2014 607, \u00a7 20, eff. June 30, 1998).\nThe confidentiality requirements of the Registry Act are further underscored in section 4(e) of the Act, which mandates that \u201c[t]he Department shall protect any information made confidential or privileged under law.\u201d 410 ILCS 525/4(e) (West 1998). Section 12 of the Registry Act similarly provides that\n\u201cAll information contained in the Registry *** shall he made available to the public upon request; provided, however, nothing in this Act permits public disclosure of any information made confidential or privileged pursuant to this Act or any other statute.\u201d 410 ILCS 525/12 (West 1998).\nThus, a review of the pertinent statutory provisions underscores that the competing interests in this case are the interest in providing public access to meaningful information about potential \u201ccancer clusters\u201d and the interest in minimizing the risk of invading the privacy of cancer patients. Indeed, these competing interests are captured in section 4(d) of the Registry Act, which prohibits the disclosure of otherwise publicly available information if it \u201ctends to lead to the identity\u201d of the cancer patients listed in the Registry.\nWe find that under either the original version of section 4(d) of the Registry Act \u2014 which applies in this case, as it was the statute in effect at the time of the occurrence \u2014 or the subsequently amended version of section 4(d), which sets forth a nonexclusive list of \u201c[f]acts that tend to lead to the identity of a person,\u201d the relevant inquiry remains the same. We must determine the meaning of the phrase \u201ctends to lead to the identity\u201d as it is used in section 4(d) of the Registry Act. Because this is an issue of statutory interpretation, our review is de novo. In re Estate of Dierkes, 191 Ill. 2d 326, 330 (2000).\nIn general, \u201ctend\u201d has been defined as meaning \u201c[t]o be disposed toward (something),\u201d to \u201cserve, contribute or conduce in some degree or way,\u201d and \u201c[t]o be directed or have a tendency to (an end, object, or purpose).\u201d Black\u2019s Law Dictionary 1479 (7th ed. 1999). In the specific context of the Registry Act, we believe that the General Assembly selected to employ the word \u201ctends\u201d in the phrase \u201ctends to lead to the identity\u201d because it is a term that is fluid and allows a case-by-case determination of whether the information at issue is subject to disclosure. We agree with the Department that the word \u201ctends\u201d is \u201cnot very precise.\u201d We observe, however, that by employing the word \u201ctends,\u201d the legislature deliberately allowed for flexibility, to the extent that, in some instances, disclosure of Registry information will be permissible and in other instances such disclosure will be prohibited. As stated above, there are competing interests \u2014 and therefore an inherent tension \u2014 within the Registry Act: the purpose of the Act is to provide the public with information about hazardous substances and cancer, while at the same time the Act is intended to protect the identity of those patients afflicted with this disease. The use of the term \u201ctends\u201d indicates that the General Assembly wished to impose a somewhat heightened standard of confidentiality by prohibiting disclosure of Registry information other than just information that simply \u201cleads to the identity\u201d of cancer patients. However, at the same time, the use of the word \u201ctends\u201d also indicates that the legislature did not intend to erect a per se bar to the disclosure of Registry information, and we must, therefore, be mindful not to interpret this term too broadly. In our view, by choosing to use the word \u201ctends,\u201d the legislature has allowed for case-specific determinations with the respect to the release of Cancer Registry information, with the analysis meant to be adaptable to the particular circumstances presented.\nHowever, we disagree with the appellate court below that, in order to preserve the intent of the legislature, the word \u201creasonably\u201d must be inserted immediately before the phrase \u201ctends to lead to the identity\u201d in section 4(d) of the Registry Act. We agree with the Department to the extent that it is neither appropriate nor necessary to insert the word \u201creasonably\u201d into section 4(d). It is apparent from the appellate court\u2019s opinions in Southern Illinoisan I and II that the addition of the word \u201creasonably\u201d by the appellate court below was driven by that court\u2019s concern that an extreme hypothetical situation could occur in which disclosure of any fact, no matter how unrelated to an individuals\u2019 identity, could \u201ctend\u201d to lead to identity of an individual listed in the Registry. In turn, the appellate court feared, any and every fact would therefore be exempt from disclosure under section 4(d). Southern Illinoisan I, 319 Ill. App. 3d at 987; see also Southern Illinoisan II, 349 Ill. App. 3d at 432. In other words, the court surmised that the word \u201ctends\u201d could lead to a per se exemption from disclosure in each and every instance. However, as stated, we do not believe that this was the intent of the legislature; rather, the intent, as we discern it, was to craft a flexible standard that would allow thoughtful consideration of each case upon its own unique facts. Accordingly, it is our belief that the purposes of the Registry Act can be achieved using its plain language without inserting additional language into section 4(d).\nIn the matter before us, the Department relies upon the testimony of Dr. Sweeney to support its position that the information requested by plaintiff is prohibited from disclosure pursuant to section 4(d) of the Registry Act because it consists of a \u201cgroup of facts that tends to lead to the identity\u201d of patients listed in the Cancer Registry. However, we find that it is not entirely clear from section 4(d) of the Registry Act whether the legislature intended that disclosure of the Registry information is prohibited upon a showing by the Department that the challenged information \u201ctends to lead to the identity\u201d of Registry patients based upon experiments conducted by experts, such as Dr. Sweeney, or if disclosure is prohibited upon a showing that the general public at large is capable of making such identifications. In other words, how revealing must the challenged information be, and to whom? Is the standard that an expert with knowledge and money can identify the Registry patients? Or is it that the general public, who may not have the same knowledge or funds, can make the identification? In addition, how much money, effort, time, and expertise must be expended? Given this uncertainty in interpretation, we are especially mindful of the public policy which underpins both the Registry Act and the FOIA: to ensure public disclosure of government information that is not otherwise protected. We also note, as stated above, that under the FOIA, public records are presumed to be open and accessible, with exceptions to disclosure to be read narrowly. Accordingly, in light of these public policies, we conclude that information \u201ctends to lead to the identity\u201d of Registry patients only if that information can be used by the general public to make those identifications.\nIn the instant matter, the Department \u2014 through the testimony of Dr. Sweeney \u2014 established that an expert with years of experience, specific knowledge of data systems, and the ability to adeptly manipulate data could identify patients listed in the Cancer Registry by using the information requested by plaintiff as one part of her multistep experiment. We note, however, that the Department failed to establish that individual members of the general public could recreate what was accomplished by Dr. Sweeney. Through Dr. Sweeney\u2019s testimony, the Department showed that a dedicated computer professional, with knowledge of unfamiliar data sets, and with $2,000 in funds to obtain the data, could identify the patients listed in the Cancer Registry. However, at trial, the Department did not adduce competent evidence of whether a nonexpert could perform the multistep procedure performed by Dr. Sweeney to identify Cancer Registry patients.\nWe note that the Department places great emphasis upon that portion of Dr. Sweeney\u2019s testimony wherein she stated her opinion that the general public could identify the patients listed in the Cancer Registry. Yet, other than Dr. Sweeney\u2019s mere conclusion, the Department adduced no proof on this point. After carefully reviewing the testimony of Dr. Sweeney, the circuit court concluded that it was her \u201cknowledge, education and experience in this area\u201d that made it possible for her to identify the Registry patients. This factual finding is not against the manifest weight of the evidence. The methodology Dr. Sweeney used to conduct her experiment was not as simple as she \u2014 or the Department \u2014 has stated. We disagree with the Department\u2019s assertion in its brief to this court that the appellate court in Southern Illinoisan II \u201csignificantly exaggerate^] [the] complexity\u201d of Dr. Sweeney\u2019s experiment. Our thorough examination of the record leads us to the conclusion that although Dr. Sweeney stated that the equipment and data sets that she used during her experiment would be readily available to the general public, the methodology she used during her experiment was unique to her education, training and experience, and not easily duplicated by the general public. We agree with the appellate court\u2019s assessment of Dr. Sweeney\u2019s testimony and, therefore, quote with some length from its opinion in Southern Illinoisan II:\n\u201cDr. Sweeney testified that she used a six-step method to identify the subjects in question. Without divulging information under seal, we note that this six-step method required knowledge that statistical information of the kind she sought existed, skill in the gathering of that information, the integration and manipulation of the information from multiple sources so that a coherent picture of the relevance of each piece of information could be formed, the analysis of the information to determine its significance to the process of identification, and the solution of the sometimes complex problems that developed during the gathering, integration and manipulation, and analysis stages. The defendants\u2019 assertions to the contrary notwithstanding, the identification process was not a simple task that almost anyone with a computer could accomplish. The process required not only the knowledge that relevant statistical data existed and the knowledge of where to look for that data but also the knowledge, education, experience, and skill to know what to do with that data once it was located \u2014 to put it all together so that it made sense. For example, Dr. Sweeney testified that at one stage in her process she examined six cases to determine what each case had in common with the others. Initially, she settled on one factor, but when she sought medical records on the basis of that factor, she got a huge number of records back and recognized that the factor in question was far too hroad to help her. That Dr. Sweeney recognized that she had made a mistake, what the mistake was, and how to correct the mistake is indicative of her level of sophistication in this field of study. We find it difficult to believe that an individual with less knowledge, education, and experience than Dr. Sweeney has would have been able to navigate the six-step process as adeptly as she did. Clearly, Dr. Sweeney\u2019s methodology required knowledge and analytical skills beyond that of the average person. The circuit court even engaged Dr. Sweeney in an extended discussion of her methodology. The trial judge stated, T want to go through the project with you step by step as if I was a computer literate person attempting to recreate what you did.\u2019 Significantly, although Dr. Sweeney\u2019s responses to this line of questioning by the court indicate in great detail how she knew what to do, her responses lack concreteness and specificity regarding the extent to which others would be able to do the same. Nor did the defendants present any other evidence on this point.\n* H* \u2756\nHad the defendants, with the many and varied resources available to a state agency, wished to present specific evidence on the extent to which other individuals possess the unique knowledge, experience, and analytical skills necessary to replicate Dr. Sweeney\u2019s work, they were free to do so. Had they chosen to bring in other witnesses who also had been able to identify the subjects from the data in question, they were free to do that as well. Had they done one or both of these things, this court would be in a better position to evaluate the threat of which the defendants complain. However, the defendants did not do so, and they now must stand by the evidence they actually presented, not by alarmist conjecture about the resounding policy implications of that somewhat limited evidence.\u201d Southern Illinoisan II, 349 Ill. App. 3d at 435-36.\nIn sum, we conclude, as did the lower courts in this matter, that the Department failed to demonstrate that the release of the Cancer Registry information requested by plaintiff tends to lead to the identity of the specific persons described in that data. As we have noted, it was the Department\u2019s burden under the FOIA to establish that its refusal to release the requested material to plaintiff fell within the exemption set forth in section 7(l)(a) of the FOIA, by establishing that the information was prohibited from disclosure pursuant to section 4(d) of the Registration Act. In the absence of more definitive proof that individuals of the general public would have the ability to duplicate Dr. Sweeney\u2019s multistep experiment, our decision is guided by the public policy of this state, which \u201cencourages a free flow and disclosure of information between government and the people.\u201d Bowie, 128 Ill. 2d at 378. As the FOIA is to be interpreted liberally, and the exemptions to disclosure are to be interpreted narrowly, we conclude that the lower courts properly instructed the Department to disclose to plaintiff the information contained in its FOIA request.\nAs a final matter, we note that in granting plaintiff access to the requested information from the Cancer Registry, the circuit court ordered plaintiff not to identify those on the Cancer Registry list. We believe that the court\u2019s order expressly forbidding plaintiff to use the information in an improper manner will ensure its confidentiality.\nCONCLUSION\nFor the foregoing reasons, the judgment of the appellate court is affirmed.\nAffirmed.\nNeuroblastoma is a cancer of the peripheral nervous system that typically develops in infants and young children. Statistics reveal that neuroblastoma afflicts approximately 9 out of every 1 million children born. See Donaldson v. Central Illinois Public Service Co., 199 Ill. 2d 63, 66 (2002).\nThe Department notes that its current Director is Dr. Eric E. Whitaker, who immediately succeeded Dr. Lumpkin in that post.\nOn the date it filed its response, the Department also filed a motion to file an amended answer. The Department requested the court to allow it to amend its answer to reflect the affirmative defenses raised in the Department\u2019s response to plaintiffs summary judgment motion and in its own cross-motion for summary judgment.",
        "type": "majority",
        "author": "JUSTICE McMORROW"
      }
    ],
    "attorneys": [
      "Lisa Madigan, Attorney General, of Springfield (Gary Feinerman, Solicitor General, and Jerald S. Post, Assistant Attorney General, of Chicago, of counsel), for appellants.",
      "Donald M. Craven, of Springfield, for appellee.",
      "Richard J. O\u2019Brien, Eric S. Mattson and Jamie L. Secord, of Sidley, Austin, Brown & Wood, L.L.P., of Chicago, for amici curiae Associated Press et al."
    ],
    "corrections": "",
    "head_matter": "(No. 98712.\nSOUTHERN ILLINOISAN, Appellee, v. THE ILLINOIS DEPARTMENT OF PUBLIC HEALTH et al., Appellants.\nOpinion filed February 2, 2006.\nLisa Madigan, Attorney General, of Springfield (Gary Feinerman, Solicitor General, and Jerald S. Post, Assistant Attorney General, of Chicago, of counsel), for appellants.\nDonald M. Craven, of Springfield, for appellee.\nRichard J. O\u2019Brien, Eric S. Mattson and Jamie L. Secord, of Sidley, Austin, Brown & Wood, L.L.P., of Chicago, for amici curiae Associated Press et al."
  },
  "file_name": "0390-01",
  "first_page_order": 400,
  "last_page_order": 437
}
