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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=15800&ordering=accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=15760&ordering=accession",
"results": [
{
"accession": "CLO:0014992",
"name": "DA05552 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0014993",
"name": "GM50194 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014994",
"name": "GM50189 cell",
"definition": "[' CHROMOSOME INSERTION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014995",
"name": "DA05555 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0014996",
"name": "GM02667 cell",
"definition": "[' MULTIPLE SULFATASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0014997",
"name": "DA05554 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0014998",
"name": "GM50192 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014999",
"name": "GM02668 cell",
"definition": "[' CHROMOSOME DELETION TURNER SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015000",
"name": "DA05562 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0015001",
"name": "GM02675 cell",
"definition": "[' DIABETES MELLITUS, JUVENILE-ONSET INSULIN-DEPENDENT; IDDM']",
"term_type": "cell line"
},
{
"accession": "CLO:0015002",
"name": "DA05563 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0015003",
"name": "GM02674 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0015004",
"name": "GM02673 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0015005",
"name": "GM02672 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE XX MALE SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015006",
"name": "GM02671 cell",
"definition": "[' XX MALE SYNDROME APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0015007",
"name": "GM02670 cell",
"definition": "[' XX MALE SYNDROME TRANSLOCATED CHROMOSOME DERIVATIVE CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015008",
"name": "GM50173 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0015009",
"name": "GM50174 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015010",
"name": "GM50175 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015011",
"name": "GM50176 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
}
]
}