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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12280&ordering=accession",
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"results": [
{
"accession": "CLO:0011472",
"name": "DA04897 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011473",
"name": "HQ00373 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0011474",
"name": "DA04899 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011475",
"name": "HQ00371 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0011476",
"name": "DA04900 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011477",
"name": "DA04901 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011478",
"name": "GM09496 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA: AUTOSOMAL DOMINANT- 166200,166210,166220, OR 166230']",
"term_type": "cell line"
},
{
"accession": "CLO:0011479",
"name": "DA04902 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011480",
"name": "GM09497 cell",
"definition": "[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']",
"term_type": "cell line"
},
{
"accession": "CLO:0011481",
"name": "GM09498 cell",
"definition": "[' GIANT CELL HEPATITIS, NEONATAL IDIOPATHIC NEONATAL HEMOCHROMATOSIS, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0011482",
"name": "DA04903 cell",
"definition": "[' DIABETES MELLITUS FAMILY SAMPLE']",
"term_type": "cell line"
},
{
"accession": "CLO:0011483",
"name": "GM09499 cell",
"definition": "[' TETRALOGY OF FALLOT MARKER CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0011484",
"name": "HQ00385 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0011485",
"name": "HQ00384 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0011486",
"name": "HQ00383 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0011487",
"name": "GM09539 cell",
"definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
"term_type": "cell line"
},
{
"accession": "CLO:0011488",
"name": "GM09536 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE NEUROFIBROMATOSIS, TYPE I; NF1']",
"term_type": "cell line"
},
{
"accession": "CLO:0011489",
"name": "GM09535 cell",
"definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
"term_type": "cell line"
},
{
"accession": "CLO:0011490",
"name": "GM09534 cell",
"definition": "[' NEUROFIBROMATOSIS, TYPE I; NF1']",
"term_type": "cell line"
},
{
"accession": "CLO:0011491",
"name": "GM09544 cell",
"definition": "[' GILLES DE LA TOURETTE SYNDROME; GTS']",
"term_type": "cell line"
}
]
}