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"results": [
{
"accession": "CLO:0002532",
"name": "CMT-93 cell",
"definition": "['disease: polyploid carcinoma']",
"term_type": "cell line"
},
{
"accession": "CLO:0002534",
"name": "C-N90 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002535",
"name": "C-N95 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002536",
"name": "CN96 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "MS:1001307",
"name": "CNBr",
"definition": "Cyanogen bromide.",
"term_type": "cleavage agent"
},
{
"accession": "CLO:0002537",
"name": "CNC 127I cell",
"definition": "['disease: mammary tumor']",
"term_type": "cell line"
},
{
"accession": "NCBITaxon:6073",
"name": "Cnidaria",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:641",
"name": "CNS demyelinating autoimmune disease",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CL:0000402",
"name": "CNS interneuron",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CL:0000117",
"name": "CNS neuron (sensu Vertebrata)",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002538",
"name": "CO 88BV59-1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002539",
"name": "Co88BV59H21-2 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0002540",
"name": "Co88BV59H21-2V67-66 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:2232",
"name": "coagulation factor deficiency",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "DOID:2212",
"name": "coagulation protein disorder",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "EFO:0000359",
"name": "Cockayne syndrome",
"definition": "['A simple genetic disease that is caused by a rare autosomal recessive mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging.', 'A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.', 'An autosomal recessive syndrome caused by mutations in the ERCC8 and ERCC6 genes. It is characterized by growth and developmental delay, vision and hearing impairment, and impairment of the peripheral nervous system function.', 'Caused by mutations of gene CKN1.', 'Caused by mutations of gene ERCC6.', 'Type C is a rare form. Its genetic defect is not clear; appears to be a heterogeneous group. OMIM suggests that Type C should not be used anymore.']",
"term_type": "cell line"
},
{
"accession": "CLO:0009959",
"name": "CoCM-1 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "UBERON:0002323",
"name": "coelemic cavity lumen",
"definition": "['The cavity within the body of all animals higher than the coelenterates and certain primitive worms, formed by the splitting of the embryonic mesoderm into two layers. In mammals it forms the peritoneal, pleural, and pericardial cavities.']",
"term_type": "cell line"
},
{
"accession": "UBERON:0011997",
"name": "coelom",
"definition": "['The aggregate of the coelemic cavity lumen plus the membranes that line the lumen.']",
"term_type": "cell line"
},
{
"accession": "UBERON:0005891",
"name": "coelomic epithelium",
"definition": "['The epithelial lining of the surface of the coelom.']",
"term_type": "cell line"
}
]
}