GET /api/ms_vocab/?format=api&offset=27060&ordering=-name
HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

{
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    "next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=27080&ordering=-name",
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    "results": [
        {
            "accession": "CLO:0030584",
            "name": "GM09887 cell",
            "definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030587",
            "name": "GM09886 cell",
            "definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030601",
            "name": "GM09885 cell",
            "definition": "[' SIALIC ACID STORAGE DISEASE; SIASD']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030599",
            "name": "GM09884 cell",
            "definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030597",
            "name": "GM09871 cell",
            "definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030596",
            "name": "GM09870 cell",
            "definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030594",
            "name": "GM09869 cell",
            "definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030592",
            "name": "GM09868 cell",
            "definition": "[' INVERTED CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030589",
            "name": "GM09867 cell",
            "definition": "[' INVERTED CHROMOSOME']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030625",
            "name": "GM09865 cell",
            "definition": "[' EPIDERMOLYSIS BULLOSA: DYSTROPHIC, JUNCTIONAL, OR SIMPLEX TYPES']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030627",
            "name": "GM09864 cell",
            "definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030619",
            "name": "GM09853 cell",
            "definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030630",
            "name": "GM09852 cell",
            "definition": "[' ICHTHYOSIS, X-LINKED']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030629",
            "name": "GM09850 cell",
            "definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030632",
            "name": "GM09849 cell",
            "definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030631",
            "name": "GM09838 cell",
            "definition": "[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030634",
            "name": "GM09834 cell",
            "definition": "[' CHROMOSOME INSERTION BASAL CELL NEVUS SYNDROME; BCNS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030633",
            "name": "GM09833 cell",
            "definition": "[' CHROMOSOME INSERTION BASAL CELL NEVUS SYNDROME; BCNS']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030636",
            "name": "GM09832 cell",
            "definition": "[' TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT']",
            "term_type": "cell line"
        },
        {
            "accession": "CLO:0030635",
            "name": "GM09830 cell",
            "definition": "[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']",
            "term_type": "cell line"
        }
    ]
}