HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17640&ordering=name",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=17600&ordering=name",
"results": [
{
"accession": "CLO:0021040",
"name": "GM11521 cell",
"definition": "[' SNP500 PANEL DRUZE POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0021039",
"name": "GM11522 cell",
"definition": "[' DRUZE POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0021038",
"name": "GM11523 cell",
"definition": "[' DRUZE POPULATION SNP500 PANEL']",
"term_type": "cell line"
},
{
"accession": "CLO:0021037",
"name": "GM11524 cell",
"definition": "[' SNP500 PANEL DRUZE POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0021036",
"name": "GM11525 cell",
"definition": "[' SNP500 PANEL CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9 DRUZE POPULATION']",
"term_type": "cell line"
},
{
"accession": "CLO:0021033",
"name": "GM11526 cell",
"definition": "[' CHROMOSOME 1 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021003",
"name": "GM11529 cell",
"definition": "[' NEUROAXONAL DYSTROPHY, INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0020997",
"name": "GM11530 cell",
"definition": "[' NEUROAXONAL DYSTROPHY, INFANTILE']",
"term_type": "cell line"
},
{
"accession": "CLO:0020998",
"name": "GM11532 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0020999",
"name": "GM11534 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021002",
"name": "GM11535 cell",
"definition": "[' ADDITIONAL HUMAN/CHINESE HAMSTER SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021010",
"name": "GM11536 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0021009",
"name": "GM11538 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0021012",
"name": "GM11540 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0021011",
"name": "GM11541 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0021005",
"name": "GM11543 cell",
"definition": "[' CHROMOSOME 16 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0021058",
"name": "GM11550 cell",
"definition": "[' COCKAYNE SYNDROME TYPE UNSPECIFIED']",
"term_type": "cell line"
},
{
"accession": "CLO:0021057",
"name": "GM11551 cell",
"definition": "[' COCKAYNE SYNDROME TYPE UNSPECIFIED']",
"term_type": "cell line"
},
{
"accession": "CLO:0021054",
"name": "GM11553 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0021053",
"name": "GM11554 cell",
"definition": "[' RETICULOSIS, FAMILIAL HISTIOCYTIC']",
"term_type": "cell line"
}
]
}