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{
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{
"accession": "CLO:0014757",
"name": "GM50112 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
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{
"accession": "CLO:0014755",
"name": "GM50113 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
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{
"accession": "CLO:0014761",
"name": "GM50116 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
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{
"accession": "CLO:0014758",
"name": "GM50118 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014750",
"name": "GM50120 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014751",
"name": "GM50121 cell",
"definition": "[' HOLOPROSENCEPHALY ISOCHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014752",
"name": "GM50122 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014753",
"name": "GM50124 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
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{
"accession": "CLO:0014669",
"name": "GM50125 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
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{
"accession": "CLO:0014670",
"name": "GM50126 cell",
"definition": "[' HOLOPROSENCEPHALY CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014672",
"name": "GM50128 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014674",
"name": "GM50129 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
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{
"accession": "CLO:0014675",
"name": "GM50139 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
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{
"accession": "CLO:0014676",
"name": "GM50142 cell",
"definition": "[' DUPLICATED CHROMOSOME']",
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"accession": "CLO:0014677",
"name": "GM50143 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014679",
"name": "GM50145 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014678",
"name": "GM50146 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014683",
"name": "GM50147 cell",
"definition": "[' DUPLICATED CHROMOSOME RECOMBINANT CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014713",
"name": "GM50149 cell",
"definition": "[' TRANSLOCATED CHROMOSOME CRI-DU-CHAT SYNDROME DERIVATIVE CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014715",
"name": "GM50150 cell",
"definition": "[' HOLOPROSENCEPHALY CHROMOSOME DELETION']",
"term_type": "cell line"
}
]
}