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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=11940&ordering=-accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=11900&ordering=-accession",
"results": [
{
"accession": "CLO:0031088",
"name": "GM18397 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0031087",
"name": "GM18407 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0031086",
"name": "GM14283 cell",
"definition": "[' OBESITY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031085",
"name": "GM14282 cell",
"definition": "[' OBESITY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031084",
"name": "GM18402 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0031083",
"name": "GM14277 cell",
"definition": "[' OBESITY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031082",
"name": "GM14274 cell",
"definition": "[' OBESITY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031081",
"name": "GM14275 cell",
"definition": "[' OBESITY']",
"term_type": "cell line"
},
{
"accession": "CLO:0031080",
"name": "GM18321 cell",
"definition": "[' SMITH-MAGENIS SYNDROME; SMS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031079",
"name": "GM18322 cell",
"definition": "[' CHROMOSOME DELETION SMITH-MAGENIS SYNDROME; SMS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031078",
"name": "GM18319 cell",
"definition": "[' SMITH-MAGENIS SYNDROME; SMS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0031077",
"name": "GM18320 cell",
"definition": "[' SMITH-MAGENIS SYNDROME; SMS CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0031076",
"name": "GM18325 cell",
"definition": "[' SMITH-MAGENIS SYNDROME; SMS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031075",
"name": "GM18323 cell",
"definition": "[' CHROMOSOME DELETION SMITH-MAGENIS SYNDROME; SMS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031074",
"name": "GM18324 cell",
"definition": "[' CHROMOSOME DELETION SMITH-MAGENIS SYNDROME; SMS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031073",
"name": "GM18311 cell",
"definition": "[' HOLOPROSENCEPHALY CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0031072",
"name": "GM18313 cell",
"definition": "[' FARBER LIPOGRANULOMATOSIS']",
"term_type": "cell line"
},
{
"accession": "CLO:0031071",
"name": "GM18310 cell",
"definition": "[' XXY SYNDROME; KLINEFELTER SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0031070",
"name": "GM18334 cell",
"definition": "[' AZOOSPERMIA FACTOR C']",
"term_type": "cell line"
},
{
"accession": "CLO:0031069",
"name": "GM18335 cell",
"definition": "[' AZOOSPERMIA FACTOR C APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
}
]
}