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"accession": "CLO:0013972",
"name": "GM21655 cell",
"definition": "[' MOSAIC VARIEGATED ANEUPLOIDY SYNDROME; MVA']",
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{
"accession": "CLO:0013973",
"name": "GM21656 cell",
"definition": "[' MOSAIC VARIEGATED ANEUPLOIDY SYNDROME; MVA']",
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{
"accession": "CLO:0013974",
"name": "ND08710 cell",
"definition": "[' EPILEPSY']",
"term_type": "cell line"
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{
"accession": "CLO:0013975",
"name": "GM21647 cell",
"definition": "[' INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA']",
"term_type": "cell line"
},
{
"accession": "CLO:0013976",
"name": "ND08720 cell",
"definition": "[' PROGRESSIVE SUPRANUCLEAR PALSY']",
"term_type": "cell line"
},
{
"accession": "CLO:0013977",
"name": "GM21648 cell",
"definition": "[' INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA (PLATE I)']",
"term_type": "cell line"
},
{
"accession": "CLO:0013978",
"name": "ND08708 cell",
"definition": "[' EPILEPSY']",
"term_type": "cell line"
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{
"accession": "CLO:0013979",
"name": "GM21649 cell",
"definition": "[' INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA (PLATE II)']",
"term_type": "cell line"
},
{
"accession": "CLO:0013980",
"name": "ND08709 cell",
"definition": "[' ASYMPTOMATIC AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL']",
"term_type": "cell line"
},
{
"accession": "CLO:0013981",
"name": "GM21650 cell",
"definition": "[' INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA INTERNATIONAL HAPMAP PROJECT - MAASAI IN KINYAWA, KENYA (PLATE II)']",
"term_type": "cell line"
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{
"accession": "CLO:0013982",
"name": "GM17161 cell",
"definition": "[' SNP500 PANEL HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
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"accession": "CLO:0013983",
"name": "GM17162 cell",
"definition": "[' HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
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"accession": "CLO:0013984",
"name": "GM17160 cell",
"definition": "[' HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
},
{
"accession": "CLO:0013985",
"name": "GM17169 cell",
"definition": "[' HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
},
{
"accession": "CLO:0013986",
"name": "GM13019 cell",
"definition": "[' CHROMOSOME DELETION TURNER SYNDROME']",
"term_type": "cell line"
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{
"accession": "CLO:0013987",
"name": "GM17168 cell",
"definition": "[' HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
},
{
"accession": "CLO:0013988",
"name": "GM12980 cell",
"definition": "[' CEPH/UTAH PEDIGREE 1427']",
"term_type": "cell line"
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{
"accession": "CLO:0013989",
"name": "GM17167 cell",
"definition": "[' SNP500 PANEL HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
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{
"accession": "CLO:0013990",
"name": "GM17166 cell",
"definition": "[' SNP500 PANEL HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 100']",
"term_type": "cell line"
},
{
"accession": "CLO:0013991",
"name": "GM13021 cell",
"definition": "[' FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC']",
"term_type": "cell line"
}
]
}