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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=23840&ordering=-accession",
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"results": [
{
"accession": "CLO:0019188",
"name": "ND14652 cell",
"definition": "[' AMYOTROPHIC LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019187",
"name": "GM12226 cell",
"definition": "[' INCONTINENTIA PIGMENTI; IP']",
"term_type": "cell line"
},
{
"accession": "CLO:0019186",
"name": "GM12228 cell",
"definition": "[' ALAGILLE SYNDROME; AGS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019185",
"name": "GM12223 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019184",
"name": "GM12222 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019183",
"name": "GM12225 cell",
"definition": "[' INCONTINENTIA PIGMENTI; IP']",
"term_type": "cell line"
},
{
"accession": "CLO:0019182",
"name": "GM12224 cell",
"definition": "[' HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019181",
"name": "GM12217 cell",
"definition": "[' ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0019180",
"name": "GM12221 cell",
"definition": "[' SPONDYLOPERIPHERAL DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019179",
"name": "GM12220 cell",
"definition": "[' SPONDYLOPERIPHERAL DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019178",
"name": "ND14672 cell",
"definition": "[' AMYOTROPHIC LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019177",
"name": "ND14673 cell",
"definition": "[' AMYOTROPHIC LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019176",
"name": "ND14674 cell",
"definition": "[' PRIMARY LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019175",
"name": "ND14675 cell",
"definition": "[' AMYOTROPHIC LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019174",
"name": "ND14676 cell",
"definition": "[' AMYOTROPHIC LATERAL SCLEROSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019173",
"name": "ND14677 cell",
"definition": "[' SPOUSAL CONTROL']",
"term_type": "cell line"
},
{
"accession": "CLO:0019172",
"name": "ND14678 cell",
"definition": "[' SPOUSAL CONTROL']",
"term_type": "cell line"
},
{
"accession": "CLO:0019171",
"name": "ND14669 cell",
"definition": "[' SPOUSAL CONTROL']",
"term_type": "cell line"
},
{
"accession": "CLO:0019170",
"name": "GM12215 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 17 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019169",
"name": "GM12214 cell",
"definition": "[' PERIPHERAL MYELIN PROTEIN 22; PMP22 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A']",
"term_type": "cell line"
}
]
}