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{
"accession": "CLO:0003627",
"name": "HC-1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037256",
"name": "HBL-1 cell",
"definition": "['HBL-1 (aka human is an EBV-negative B-cell lymphoma cell line established from the pleural effusion of a patient with malignant lymphoma, diffuse, large cell.']",
"term_type": "cell line"
},
{
"accession": "CLO:0003626",
"name": "HBL-100 cell",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "CLO:0003624",
"name": "HBE4-E6/E7 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003625",
"name": "HBE4-E6/E7-C1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003623",
"name": "HBE135-E6E7 cell",
"definition": "['disease: HPV-16 E6/E7 transformed']",
"term_type": "cell line"
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{
"accession": "CLO:0003622",
"name": "HB cell",
"definition": "['disease: epidermolysis bullosa simplex']",
"term_type": "cell line"
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{
"accession": "DOID:1060",
"name": "Hartnup disease",
"definition": "['\"An inborn metabolic brain disease that is the result of an inherited metabolic disease that is caused by abnormalities of the renal tubules and is characterized especially by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular incoordination due to the effects of the disease on the cerebellum.\" [url:http\\\\://www2.merriam-webster.com/cgi-bin/mwmednlm?book=Medical&va=Hartnup]']",
"term_type": "cell line"
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{
"accession": "CLO:0009998",
"name": "HARA cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003621",
"name": "HAP-T1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CL:0000413",
"name": "haploid cell",
"definition": "['A cell whose nucleus contains a single haploid genome.']",
"term_type": "cell line"
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{
"accession": "PATO:0001375",
"name": "haploid",
"definition": "[\"A ploidy quality inhering in a bearer by virtue of the bearer's containing a single set of homologous chromosomes.\"]",
"term_type": "cell line"
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{
"accession": "NCBITaxon:13557",
"name": "Hapalemur griseus",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "DOID:3462",
"name": "hamartoma",
"definition": "[]",
"term_type": "cell line"
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{
"accession": "DOID:3981",
"name": "Hallervorden-Spatz syndrome",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0037391",
"name": "hAKPC-P cell",
"definition": "['human Amniotic-fluid Kidney Progenitor Cells-Podocyte']",
"term_type": "cell line"
},
{
"accession": "CLO:0003620",
"name": "HaK cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "UBERON:0000329",
"name": "hair root",
"definition": "['The enlarged basal part of a hair within the skin[BTO]. The root of the hair ends in an enlargement, the hair bulb, which is whiter in color and softer in texture than the shaft, and is lodged in a follicular involution of the epidermis called the hair follicle. [Wikipedia].']",
"term_type": "cell line"
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{
"accession": "DOID:421",
"name": "hair disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003615",
"name": "Ha Fe cell",
"definition": "[]",
"term_type": "cell line"
}
]
}