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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12840&ordering=accession",
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"results": [
{
"accession": "CLO:0012032",
"name": "HQ00512 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012033",
"name": "GM09246 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012034",
"name": "HQ00509 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012035",
"name": "HQ00510 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012036",
"name": "GM09252 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012037",
"name": "GM09237 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012038",
"name": "GM09236 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012039",
"name": "GM09239 cell",
"definition": "[' PORPHYRIA, ACUTE INTERMITTENT']",
"term_type": "cell line"
},
{
"accession": "CLO:0012040",
"name": "GM09238 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012041",
"name": "GM09292 cell",
"definition": "[' RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012042",
"name": "GM09293 cell",
"definition": "[' RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012043",
"name": "GM09290 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012044",
"name": "GM09291 cell",
"definition": "[' RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012045",
"name": "GM09287 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - TRISOMY 9 ANEUPLOID CHROMOSOME NUMBER - TRISOMY']",
"term_type": "cell line"
},
{
"accession": "CLO:0012046",
"name": "HQ00513 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012047",
"name": "HQ00514 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012048",
"name": "HQ00515 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012049",
"name": "HQ00516 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012050",
"name": "HQ00517 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012051",
"name": "HQ00518 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
}
]
}