{
    "title": "Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.",
    "journal": "Nature genetics",
    "date": "1999",
    "authors": "Brooks-Wilson A, Marcil M, Clee SM, Zhang LH, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HO, Loubser O, Ouelette BF, Fichter K, Ashbourne-Excoffon KJ, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone S, Kastelein JJ, Genest J Jr, Hayden MR",
    "reference": {
        "type": "PubMed",
        "id": "10431236",
        "url": "https://pubmed.ncbi.nlm.nih.gov/10431236"
    },
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    "referenced_proteins": [
        {
            "uniprot_canonical_ac": "O95477-1",
            "protein_name": "Phospholipid-transporting ATPase ABCA1",
            "gene_name": "ABCA1",
            "tax_name": "Human"
        },
        {
            "uniprot_canonical_ac": "P02647-1",
            "protein_name": "Apolipoprotein A-I",
            "gene_name": "APOA1",
            "tax_name": "Human"
        }
    ],
    "species": [
        {
            "name": "Homo sapiens",
            "taxid": 9606,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O95477",
                    "url": "https://www.uniprot.org/uniprot/O95477"
                }
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            "common_name": "Human",
            "glygen_name": "Human",
            "reference_species": "Homo sapiens [9606]"
        }
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    "record_id": "pubmed.10431236",
    "abstract": "",
    "glycosylation": [],
    "mutagenesis": [],
    "snv": [],
    "phosphorylation": [],
    "glycation": [],
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