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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=14380&ordering=accession",
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"results": [
{
"accession": "CLO:0013572",
"name": "HQ00231 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013573",
"name": "GM03129 cell",
"definition": "[' METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013574",
"name": "HQ00224 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013575",
"name": "GM03130 cell",
"definition": "[' METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013576",
"name": "HQ00225 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013577",
"name": "GM03127 cell",
"definition": "[' PSEUDOACHONDROPLASTIC DYSPLASIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0013578",
"name": "HQ00226 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013579",
"name": "GM03128 cell",
"definition": "[' GLYCOGEN STORAGE DISEASE VII']",
"term_type": "cell line"
},
{
"accession": "CLO:0013580",
"name": "HQ00227 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013581",
"name": "HQ00218 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013582",
"name": "HQ00221 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0013583",
"name": "GM03120 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013584",
"name": "GM03119 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0013585",
"name": "GM03126 cell",
"definition": "[' TETRALOGY OF FALLOT CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0013586",
"name": "GM03125 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0013587",
"name": "GM03124 cell",
"definition": "[' NIEMANN-PICK DISEASE, TYPE C1; NPC1 NPC1 GENE; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0013588",
"name": "GM03123 cell",
"definition": "[' NPC1 GENE; NPC1 NIEMANN-PICK DISEASE, TYPE C1; NPC1']",
"term_type": "cell line"
},
{
"accession": "CLO:0013589",
"name": "GM13182 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
},
{
"accession": "CLO:0013590",
"name": "GM13183 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
},
{
"accession": "CLO:0013591",
"name": "GM13184 cell",
"definition": "[' CEPH/VENEZUELAN PEDIGREE 102']",
"term_type": "cell line"
}
]
}