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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=16320&ordering=name",
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"results": [
{
"accession": "CLO:0010649",
"name": "GM09087 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0010646",
"name": "GM09089 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0010647",
"name": "GM09090 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0010662",
"name": "GM09091 cell",
"definition": "[' POLYCYSTIC KIDNEYS']",
"term_type": "cell line"
},
{
"accession": "CLO:0010652",
"name": "GM09093 cell",
"definition": "[' ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF']",
"term_type": "cell line"
},
{
"accession": "CLO:0010653",
"name": "GM09099 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0010654",
"name": "GM09100 cell",
"definition": "[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2']",
"term_type": "cell line"
},
{
"accession": "CLO:0010655",
"name": "GM09101 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010656",
"name": "GM09102 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0010657",
"name": "GM09110 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010658",
"name": "GM09112 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010659",
"name": "GM09113 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010660",
"name": "GM09115 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010661",
"name": "GM09116 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010623",
"name": "GM09117 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010621",
"name": "GM09118 cell",
"definition": "[' ORNITHINE AMINOTRANSFERASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0010622",
"name": "GM09132 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0010629",
"name": "GM09133 cell",
"definition": "[' CHROMOSOME DELETION PRADER-WILLI SYNDROME; PWS']",
"term_type": "cell line"
},
{
"accession": "CLO:0010630",
"name": "GM09138 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0010627",
"name": "GM09142 cell",
"definition": "[' CHROMOSOME 21 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
}
]
}