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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=16920&ordering=-accession",
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"results": [
{
"accession": "CLO:0026108",
"name": "GM00451 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026107",
"name": "GM00450 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026106",
"name": "GM00452 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026105",
"name": "GM00447 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026104",
"name": "GM00445 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026103",
"name": "GM00449 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC']",
"term_type": "cell line"
},
{
"accession": "CLO:0026102",
"name": "GM00448 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026101",
"name": "GM00442 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE GALACTOSEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0026100",
"name": "GM00444 cell",
"definition": "[' PYRUVATE CARBOXYLASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0026099",
"name": "GM00443 cell",
"definition": "[' GLUCOSIDASE, ALPHA, ACID; GAA GLYCOGEN STORAGE DISEASE II']",
"term_type": "cell line"
},
{
"accession": "CLO:0026098",
"name": "GM11403 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0026097",
"name": "GM11402 cell",
"definition": "[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']",
"term_type": "cell line"
},
{
"accession": "CLO:0026096",
"name": "GM11401 cell",
"definition": "[' MATURITY-ONSET DIABETES OF THE YOUNG, TYPE I; MODY1']",
"term_type": "cell line"
},
{
"accession": "CLO:0026095",
"name": "GM11397 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0026094",
"name": "GM11405 cell",
"definition": "[' ANGELMAN SYNDROME; AS']",
"term_type": "cell line"
},
{
"accession": "CLO:0026093",
"name": "GM11404 cell",
"definition": "[' ANGELMAN SYNDROME; AS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0026092",
"name": "GM11394 cell",
"definition": "[' EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 3; ERCC3 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB']",
"term_type": "cell line"
},
{
"accession": "CLO:0026091",
"name": "GM11393 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS']",
"term_type": "cell line"
},
{
"accession": "CLO:0026090",
"name": "GM11392 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS']",
"term_type": "cell line"
},
{
"accession": "CLO:0026089",
"name": "GM11391 cell",
"definition": "[' PRADER-WILLI SYNDROME; PWS']",
"term_type": "cell line"
}
]
}