Ms Unique Vocabularies List

HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

{
    "count": 43797,
    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12700&ordering=accession",
    "previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12660&ordering=accession",
    "results": [
        {
            "accession": "CLO:0011892",
            "name": "DA05036 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011893",
            "name": "HQ00529 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011894",
            "name": "HQ00528 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011895",
            "name": "DA05037 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011896",
            "name": "DA05038 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011897",
            "name": "HQ00527 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011898",
            "name": "DA05039 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011899",
            "name": "HQ00526 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011900",
            "name": "HQ00525 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011901",
            "name": "DA05040 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011902",
            "name": "HQ00524 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011903",
            "name": "DA05041 cell",
            "definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011904",
            "name": "HQ00534 cell",
            "definition": "[' HUNTINGTON DISEASE; HD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011905",
            "name": "GM09317 cell",
            "definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011906",
            "name": "GM09316 cell",
            "definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011907",
            "name": "GM09311 cell",
            "definition": "[' GILLES DE LA TOURETTE SYNDROME; GTS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011908",
            "name": "GM09329 cell",
            "definition": "[' GILLES DE LA TOURETTE SYNDROME; GTS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011909",
            "name": "GM09326 cell",
            "definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC XYY SYNDROME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011910",
            "name": "GM09325 cell",
            "definition": "[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0011911",
            "name": "GM09324 cell",
            "definition": "[' OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL INVERTED CHROMOSOME']",
            "term_type": "cell line"
        }
    ]
}