Ms Unique Vocabularies List

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{
    "count": 43797,
    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=180&ordering=-name",
    "previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=140&ordering=-name",
    "results": [
        {
            "accession": "CLO:0009615",
            "name": "WM-266-4 cell",
            "definition": "['disease: melanoma (skin primary)']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009612",
            "name": "WM 266-4 cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009614",
            "name": "WM1552C cell",
            "definition": "['disease: primary superficial spreading melanoma   in radial growth phase/vertical growth phase']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009613",
            "name": "WM-115 cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009611",
            "name": "WM 1043 cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009610",
            "name": "WKD cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "DOID:9169",
            "name": "Wiskott-Aldrich syndrome",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009609",
            "name": "WISH cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009608",
            "name": "Win Mec cell",
            "definition": "['disease: xeroderma pigmentosum, presumed   heterozygote']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009607",
            "name": "WI-MN-1 cell",
            "definition": "['disease: hybridoma']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009606",
            "name": "WILCL cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009605",
            "name": "WIL2-S cell",
            "definition": "['disease: hybridoma fusion partner']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009604",
            "name": "WIL2-NS cell",
            "definition": "['disease: hybridoma fusion partner']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009601",
            "name": "WIL2 NS cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009602",
            "name": "WIL2.NS.6TG cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009603",
            "name": "WI-L2-729HF2 cell",
            "definition": "['disease: hybridoma fusion partner']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009600",
            "name": "WiDr cell",
            "definition": "['disease: colorectal adenocarcinoma']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009598",
            "name": "WI-38 VA-13 subline 2R cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009599",
            "name": "WI-38 VA-13 Subline 2RA cell",
            "definition": "[]",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0009597",
            "name": "WI-38 VA-13 cell",
            "definition": "[]",
            "term_type": "cell line"
        }
    ]
}