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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=22980&ordering=name",
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"results": [
{
"accession": "CLO:0014983",
"name": "GM50186 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014994",
"name": "GM50189 cell",
"definition": "[' CHROMOSOME INSERTION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014998",
"name": "GM50192 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014989",
"name": "GM50193 cell",
"definition": "[' 18P- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014993",
"name": "GM50194 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014977",
"name": "GM50291 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014978",
"name": "GM50292 cell",
"definition": "[' 18P- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014976",
"name": "GM50321 cell",
"definition": "[' 18P- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012521",
"name": "GM50322 cell",
"definition": "[' CHROMOSOME DELETION 18P- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012520",
"name": "GM50323 cell",
"definition": "[' ISOCHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012519",
"name": "GM50332 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012518",
"name": "GM50333 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012526",
"name": "GM50334 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012525",
"name": "GM50336 cell",
"definition": "[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']",
"term_type": "cell line"
},
{
"accession": "CLO:0012523",
"name": "GM50345 cell",
"definition": "[' CEREBROOCULOFACIOSKELETAL SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0012522",
"name": "GM50346 cell",
"definition": "[' CEREBROOCULOFACIOSKELETAL SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0003536",
"name": "GM7372 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003537",
"name": "GM7373 cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003538",
"name": "GM86 Clone 745A cell",
"definition": "[]",
"term_type": "cell line"
},
{
"accession": "CLO:0003539",
"name": "GM87 cell",
"definition": "[]",
"term_type": "cell line"
}
]
}