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{
"accession": "CLO:0013655",
"name": "GM13138 cell",
"definition": "[' GLYCOGEN STORAGE DISEASE II']",
"term_type": "cell line"
},
{
"accession": "CLO:0013668",
"name": "GM13139 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013667",
"name": "GM13140 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013670",
"name": "GM13141 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013669",
"name": "GM13142 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013671",
"name": "GM13147 cell",
"definition": "[' CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0013625",
"name": "GM13148 cell",
"definition": "[' CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0013627",
"name": "GM13154 cell",
"definition": "[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']",
"term_type": "cell line"
},
{
"accession": "CLO:0013622",
"name": "GM13155 cell",
"definition": "[' XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES']",
"term_type": "cell line"
},
{
"accession": "CLO:0013623",
"name": "GM13157 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 16 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013620",
"name": "GM13158 cell",
"definition": "[' CHROMOSOME 10 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS CHROMOSOME 16 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013621",
"name": "GM13159 cell",
"definition": "[' CHROMOSOME 16 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013650",
"name": "GM13160 cell",
"definition": "[' CHROMOSOME 16 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013648",
"name": "GM13161 cell",
"definition": "[' CHROMOSOME 16 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013645",
"name": "GM13164 cell",
"definition": "[' RUBINSTEIN-TAYBI SYNDROME; RSTS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013643",
"name": "GM13166 cell",
"definition": "[' TURNER SYNDROME ISOCHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013593",
"name": "GM13175 cell",
"definition": "[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 1 SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0013594",
"name": "GM13180 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
},
{
"accession": "CLO:0013596",
"name": "GM13181 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
},
{
"accession": "CLO:0013589",
"name": "GM13182 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
}
]
}