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{
"accession": "CLO:0012338",
"name": "GM17421 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012254",
"name": "GM17420 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012256",
"name": "GM17419 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012262",
"name": "GM17418 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012263",
"name": "GM17417 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']",
"term_type": "cell line"
},
{
"accession": "CLO:0012266",
"name": "GM17416 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0012294",
"name": "GM17415 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0012293",
"name": "GM17414 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0012296",
"name": "GM17413 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0012295",
"name": "GM17412 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0012299",
"name": "GM17411 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0012217",
"name": "GM17410 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0012221",
"name": "GM17400 cell",
"definition": "[' REFSUM DISEASE, INFANTILE FORM RETINITIS PIGMENTOSA 1; RP1']",
"term_type": "cell line"
},
{
"accession": "CLO:0012211",
"name": "GM17398 cell",
"definition": "[' ZELLWEGER SYNDROME; ZS PEROXISOME BIOGENESIS FACTOR 26; PEX26']",
"term_type": "cell line"
},
{
"accession": "CLO:0012216",
"name": "GM17396 cell",
"definition": "[' HUMAN VARIATION PANEL - MEXICAN INDIAN']",
"term_type": "cell line"
},
{
"accession": "CLO:0012207",
"name": "GM17395 cell",
"definition": "[' HUMAN VARIATION PANEL - MEXICAN INDIAN']",
"term_type": "cell line"
},
{
"accession": "CLO:0012209",
"name": "GM17394 cell",
"definition": "[' HUMAN VARIATION PANEL - MEXICAN INDIAN']",
"term_type": "cell line"
},
{
"accession": "CLO:0012246",
"name": "GM17393 cell",
"definition": "[' HUMAN VARIATION PANEL - MEXICAN INDIAN']",
"term_type": "cell line"
},
{
"accession": "CLO:0012245",
"name": "GM17392 cell",
"definition": "[' HUMAN VARIATION PANEL - MEXICAN INDIAN']",
"term_type": "cell line"
},
{
"accession": "CLO:0012244",
"name": "GM17391 cell",
"definition": "[' SNP500 PANEL HUMAN VARIATION PANEL - PACIFIC']",
"term_type": "cell line"
}
]
}