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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=37700&ordering=accession",
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"results": [
{
"accession": "CLO:0036892",
"name": "GM07152 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036893",
"name": "AG01440 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036894",
"name": "AG01178 cell",
"definition": "[' HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0036895",
"name": "GM07157 cell",
"definition": "[' PELIZAEUS-MERZBACHER DISEASE; PMD']",
"term_type": "cell line"
},
{
"accession": "CLO:0036896",
"name": "GM07158 cell",
"definition": "[' TRANSLOCATED CHROMOSOME FUMARATE HYDRATASE; FH']",
"term_type": "cell line"
},
{
"accession": "CLO:0036897",
"name": "AG01437 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036898",
"name": "GM07155 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036899",
"name": "AG00990 cell",
"definition": "[' SEIP SYNDROME LAMIN A/C; LMNA']",
"term_type": "cell line"
},
{
"accession": "CLO:0036900",
"name": "GM07156 cell",
"definition": "[' PELIZAEUS-MERZBACHER DISEASE; PMD']",
"term_type": "cell line"
},
{
"accession": "CLO:0036901",
"name": "GM07166 cell",
"definition": "[' NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 NIJMEGEN BREAKAGE SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036902",
"name": "AG01522 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036903",
"name": "AG01520 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036904",
"name": "AG01521 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036905",
"name": "GM07173 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0036906",
"name": "GM07172 cell",
"definition": "[' EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE']",
"term_type": "cell line"
},
{
"accession": "CLO:0036907",
"name": "GM07200 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036908",
"name": "GM07201 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036909",
"name": "GM07205 cell",
"definition": "[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']",
"term_type": "cell line"
},
{
"accession": "CLO:0036910",
"name": "GM07206 cell",
"definition": "[' EHLERS-DANLOS SYNDROME, TYPE VI']",
"term_type": "cell line"
},
{
"accession": "CLO:0036911",
"name": "GM07174 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
}
]
}