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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=14200&ordering=accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=14160&ordering=accession",
"results": [
{
"accession": "CLO:0013392",
"name": "GM03201 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0013393",
"name": "GM03206 cell",
"definition": "[' MECKEL SYNDROME; MKS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013394",
"name": "GM03208 cell",
"definition": "[' DYSTONIA MUSCULORUM DEFORMANS 2; DYT2']",
"term_type": "cell line"
},
{
"accession": "CLO:0013395",
"name": "GM03194 cell",
"definition": "[' DYSKERATOSIS CONGENITA; DKC']",
"term_type": "cell line"
},
{
"accession": "CLO:0013396",
"name": "HQ00124 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013397",
"name": "GM03195 cell",
"definition": "[' DYSKERATOSIS CONGENITA; DKC']",
"term_type": "cell line"
},
{
"accession": "CLO:0013398",
"name": "GM03196 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013399",
"name": "GM03197 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013400",
"name": "HQ00129 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013401",
"name": "HQ00127 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013402",
"name": "HQ00126 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013403",
"name": "HQ00125 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013404",
"name": "HQ00133 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013405",
"name": "HQ00132 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013406",
"name": "HQ00131 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013407",
"name": "HQ00130 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013408",
"name": "HQ00134 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013409",
"name": "GM03178 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0013410",
"name": "GM03189 cell",
"definition": "[' ATAXIA-TELANGIECTASIA; AT ATAXIA-TELANGIECTASIA MUTATED GENE; ATM']",
"term_type": "cell line"
},
{
"accession": "CLO:0013411",
"name": "GM03190 cell",
"definition": "[' HLA HISTOCOMPATIBILITY TYPE: 142800 THROUGH 142860 & 142880']",
"term_type": "cell line"
}
]
}