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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=12040&ordering=-accession",
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"results": [
{
"accession": "CLO:0030988",
"name": "GM01712 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0030987",
"name": "GM01715 cell",
"definition": "[' ADENOSINE DEAMINASE; ADA SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0030986",
"name": "GM01720 cell",
"definition": "[' NEURAMINIDASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0030985",
"name": "GM01719 cell",
"definition": "[' NEURAMINIDASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0030984",
"name": "GM01718 cell",
"definition": "[' NEURAMINIDASE DEFICIENCY']",
"term_type": "cell line"
},
{
"accession": "CLO:0030983",
"name": "GM01717 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0030982",
"name": "GM01726 cell",
"definition": "[' BASAL CELL NEVUS SYNDROME; BCNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0030981",
"name": "GM01725 cell",
"definition": "[' BASAL CELL NEVUS SYNDROME; BCNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0030980",
"name": "GM01723 cell",
"definition": "[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']",
"term_type": "cell line"
},
{
"accession": "CLO:0030979",
"name": "GM01721 cell",
"definition": "[' ANDROGEN RECEPTOR; AR']",
"term_type": "cell line"
},
{
"accession": "CLO:0030978",
"name": "GM01696 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030977",
"name": "GM01704 cell",
"definition": "[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']",
"term_type": "cell line"
},
{
"accession": "CLO:0030976",
"name": "GM01706 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0030975",
"name": "GM01707 cell",
"definition": "[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR CYSTIC FIBROSIS; CF']",
"term_type": "cell line"
},
{
"accession": "CLO:0030974",
"name": "GM01708 cell",
"definition": "[' CYSTIC FIBROSIS; CF']",
"term_type": "cell line"
},
{
"accession": "CLO:0030973",
"name": "GM01700 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030972",
"name": "GM01701 cell",
"definition": "[' WOLFRAM SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0030971",
"name": "GM01702 cell",
"definition": "[' GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED)']",
"term_type": "cell line"
},
{
"accession": "CLO:0030970",
"name": "GM01703 cell",
"definition": "[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']",
"term_type": "cell line"
},
{
"accession": "CLO:0030969",
"name": "GM01709 cell",
"definition": "[' DICENTRIC CHROMOSOME GONADAL DYSGENESIS']",
"term_type": "cell line"
}
]
}