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{
"count": 43797,
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"results": [
{
"accession": "CHEBI:77746",
"name": "human metabolite",
"definition": "['Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).']",
"term_type": "cell line"
},
{
"accession": "CLO:0037296",
"name": "human ovarian cancer cell line cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037335",
"name": "human stem cell line cell",
"definition": "['A stem cell line cell that is derived from human.']",
"term_type": "cell line"
},
{
"accession": "CLO:0037340",
"name": "human tissue donor",
"definition": "['A human thoat donotes tissue']",
"term_type": "cell line"
},
{
"accession": "GO:0006959",
"name": "humoral immune response",
"definition": "['An immune response mediated through a body fluid.']",
"term_type": "cell line"
},
{
"accession": "CLO:0004298",
"name": "HuNS1 cell",
"definition": "['disease: hybridoma fusion partner']",
"term_type": "cell line"
},
{
"accession": "EFO:0000533",
"name": "Huntington's disease",
"definition": "['A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea.', 'A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)']",
"term_type": "cell line"
},
{
"accession": "CLO:0009875",
"name": "HuO9 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0009876",
"name": "HuO9N2 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037394",
"name": "HUPEC 001 G0/G0 cell",
"definition": "['This cell was derived from an African American who had focal segmental glomerulosclerosis']",
"term_type": "cell line"
},
{
"accession": "CLO:0037395",
"name": "HUPEC 002 FSGS G0/G0 cell",
"definition": "['This cell was derived from an African American who had focal segmental glomerulosclerosis']",
"term_type": "cell line"
},
{
"accession": "CLO:0037396",
"name": "HUPEC 003 FSGS G0/G0 cell",
"definition": "['This cell was derived from an African American who had focal segmental glomerulosclerosis']",
"term_type": "cell line"
},
{
"accession": "CLO:0037397",
"name": "HUPEC 005 FSGS G1/G2 cell",
"definition": "['This cell was derived from an African American who had focal segmental glomerulosclerosis']",
"term_type": "cell line"
},
{
"accession": "CLO:0004299",
"name": "HuP-T3 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0004300",
"name": "HUP-T3 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0004301",
"name": "HuP-T4 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0004302",
"name": "HUP-T4 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0004303",
"name": "HuT 102 cell",
"definition": "['disease: lymphoma; mycosis fungoides']",
"term_type": "cell line"
},
{
"accession": "CLO:0004304",
"name": "HuT 78 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0004305",
"name": "HuTu 80 cell",
"definition": "[]",
"term_type": "cell line"
}
]
}