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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=26760&ordering=-name",
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"results": [
{
"accession": "CLO:0024243",
"name": "GM10501 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME X REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024244",
"name": "GM10500 cell",
"definition": "[' CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 15 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024249",
"name": "GM10498 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024248",
"name": "GM10497 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: AUTOSOMAL DOMINANT- 166200,166210,166220, OR 166230']",
"term_type": "cell line"
},
{
"accession": "CLO:0024247",
"name": "GM10496 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024250",
"name": "GM10495 cell",
"definition": "[' SNP500 PANEL PYGMY POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024251",
"name": "GM10494 cell",
"definition": "[' SNP500 PANEL PYGMY POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0024252",
"name": "GM10493 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024253",
"name": "GM10492 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0024254",
"name": "GM10490 cell",
"definition": "[' ADRENAL HYPOPLASIA WITH ADDITIONAL CONGENITAL MALFORMATIONS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024255",
"name": "GM10489 cell",
"definition": "[' ADRENAL HYPOPLASIA WITH ADDITIONAL CONGENITAL MALFORMATIONS']",
"term_type": "cell line"
},
{
"accession": "CLO:0024256",
"name": "GM10486 cell",
"definition": "[' MARFAN SYNDROME; MFS']",
"term_type": "cell line"
},
{
"accession": "CLO:0028498",
"name": "GM10482 cell",
"definition": "[' CHROMOSOME 11 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0028480",
"name": "GM10479 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0028484",
"name": "GM10478 cell",
"definition": "[' ADDITIONAL HUMAN/MOUSE SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0028475",
"name": "GM10474 cell",
"definition": "[' HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510']",
"term_type": "cell line"
},
{
"accession": "CLO:0028478",
"name": "GM10473 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0028493",
"name": "GM10472 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0028495",
"name": "GM10471 cell",
"definition": "[' PYGMY POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0028486",
"name": "GM10470 cell",
"definition": "[' PYGMY POPULATION SNP500 PANEL']",
"term_type": "cell line"
}
]
}