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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=23580&ordering=-accession",
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"results": [
{
"accession": "CLO:0019448",
"name": "GM16262 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019447",
"name": "GM16260 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019446",
"name": "GM16248 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019445",
"name": "GM16247 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0019444",
"name": "GM16245 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 7 SOMATIC CELL HYBRIDS CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0019443",
"name": "GM16269 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0019442",
"name": "GM16267 cell",
"definition": "[' HEMOGLOBIN--BETA LOCUS; HBB SICKLE CELL ANEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019441",
"name": "GM16271 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0019440",
"name": "GM16270 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0019439",
"name": "GM16266 cell",
"definition": "[' HEMOGLOBIN--BETA LOCUS; HBB SICKLE CELL ANEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0019438",
"name": "GM16265 cell",
"definition": "[' SICKLE CELL ANEMIA HEMOGLOBIN--BETA LOCUS; HBB']",
"term_type": "cell line"
},
{
"accession": "CLO:0019437",
"name": "GM12268 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418']",
"term_type": "cell line"
},
{
"accession": "CLO:0019436",
"name": "GM12267 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418']",
"term_type": "cell line"
},
{
"accession": "CLO:0019435",
"name": "GM12266 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418']",
"term_type": "cell line"
},
{
"accession": "CLO:0019434",
"name": "GM12265 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418']",
"term_type": "cell line"
},
{
"accession": "CLO:0019433",
"name": "GM16347 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD)']",
"term_type": "cell line"
},
{
"accession": "CLO:0019432",
"name": "GM12272 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE II) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]']",
"term_type": "cell line"
},
{
"accession": "CLO:0019431",
"name": "GM16272 cell",
"definition": "[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']",
"term_type": "cell line"
},
{
"accession": "CLO:0019430",
"name": "GM12271 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1418']",
"term_type": "cell line"
},
{
"accession": "CLO:0019429",
"name": "GM16349 cell",
"definition": "[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN (FSHD) TURNER SYNDROME']",
"term_type": "cell line"
}
]
}