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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=30500&ordering=-accession",
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"results": [
{
"accession": "CLO:0012528",
"name": "GM02963 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012527",
"name": "GM02962 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA: GENETICS UNCERTAIN; LETHAL']",
"term_type": "cell line"
},
{
"accession": "CLO:0012526",
"name": "GM50334 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012525",
"name": "GM50336 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012524",
"name": "GM02984 cell",
"definition": "[' EPIDERMODYSPLASIA VERRUCIFORMIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0012523",
"name": "GM50345 cell",
"definition": "[' CEREBROOCULOFACIOSKELETAL SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012522",
"name": "GM50346 cell",
"definition": "[' CEREBROOCULOFACIOSKELETAL SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012521",
"name": "GM50322 cell",
"definition": "[' CHROMOSOME DELETION 18P- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012520",
"name": "GM50323 cell",
"definition": "[' ISOCHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012519",
"name": "GM50332 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012518",
"name": "GM50333 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012517",
"name": "HQ00001 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012516",
"name": "HQ00002 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012515",
"name": "GM02968 cell",
"definition": "[' HEXOSAMINIDASE A; HEXA TAY-SACHS DISEASE; TSD']",
"term_type": "cell line"
},
{
"accession": "CLO:0012514",
"name": "GM02975 cell",
"definition": "[' FANCONI ANEMIA COMPLEMENTATION GROUP UNDETERMINED']",
"term_type": "cell line"
},
{
"accession": "CLO:0012513",
"name": "GM02973 cell",
"definition": "[' EPIDERMODYSPLASIA VERRUCIFORMIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0012512",
"name": "GM02972 cell",
"definition": "[' EPIDERMODYSPLASIA VERRUCIFORMIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0012511",
"name": "GM02971 cell",
"definition": "[' RETINOBLASTOMA, SPORADIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012510",
"name": "GM02980 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0012509",
"name": "GM02979 cell",
"definition": "[' FUCOSYLTRANSFERASE 1; FUT1']",
"term_type": "cell line"
}
]
}