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{
"accession": "CLO:0016962",
"name": "GM17589 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016988",
"name": "GM17588 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016987",
"name": "GM17587 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016984",
"name": "GM17586 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016983",
"name": "GM17583 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016986",
"name": "GM17579 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016985",
"name": "GM17578 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016979",
"name": "GM17577 cell",
"definition": "[' COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4']",
"term_type": "cell line"
},
{
"accession": "CLO:0016980",
"name": "GM17576 cell",
"definition": "[' OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 COLLAGEN, TYPE I, ALPHA-2; COL1A2']",
"term_type": "cell line"
},
{
"accession": "CLO:0016981",
"name": "GM17575 cell",
"definition": "[' CYSTINURIA; CSNU SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1']",
"term_type": "cell line"
},
{
"accession": "CLO:0016982",
"name": "GM17572 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0013033",
"name": "GM17571 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0013039",
"name": "GM17570 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0013037",
"name": "GM17569 cell",
"definition": "[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG']",
"term_type": "cell line"
},
{
"accession": "CLO:0013028",
"name": "GM17567 cell",
"definition": "[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']",
"term_type": "cell line"
},
{
"accession": "CLO:0013025",
"name": "GM17566 cell",
"definition": "[' BRUTON AGAMMAGLOBULINEMIA TYROSINE KINASE; BTK']",
"term_type": "cell line"
},
{
"accession": "CLO:0013031",
"name": "GM17557 cell",
"definition": "[' IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2']",
"term_type": "cell line"
},
{
"accession": "CLO:0013029",
"name": "GM17552 cell",
"definition": "[' IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2']",
"term_type": "cell line"
},
{
"accession": "CLO:0013019",
"name": "GM17547 cell",
"definition": "[' BRUTON AGAMMAGLOBULINEMIA TYROSINE KINASE; BTK']",
"term_type": "cell line"
},
{
"accession": "CLO:0013020",
"name": "GM17540 cell",
"definition": "[' METHYL-CPG-BINDING PROTEIN 2; MECP2 RETT SYNDROME; RTT']",
"term_type": "cell line"
}
]
}