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{
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{
"accession": "CLO:0015010",
"name": "GM50175 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015009",
"name": "GM50174 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015008",
"name": "GM50173 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0015028",
"name": "GM50172 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0015026",
"name": "GM50171 cell",
"definition": "[' INVERTED CHROMOSOME CRI-DU-CHAT SYNDROME DERIVATIVE CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015021",
"name": "GM50170 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015018",
"name": "GM50168 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0015017",
"name": "GM50167 cell",
"definition": "[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0015015",
"name": "GM50165 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014721",
"name": "GM50164 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014722",
"name": "GM50163 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014717",
"name": "GM50160 cell",
"definition": "[' 18Q- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014716",
"name": "GM50159 cell",
"definition": "[' DUPLICATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014719",
"name": "GM50158 cell",
"definition": "[' DERIVATIVE CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014718",
"name": "GM50154 cell",
"definition": "[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014710",
"name": "GM50153 cell",
"definition": "[' CHROMOSOME DELETION 18Q- SYNDROME']",
"term_type": "cell line"
},
{
"accession": "CLO:0014709",
"name": "GM50152 cell",
"definition": "[' 18P- SYNDROME CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0014715",
"name": "GM50150 cell",
"definition": "[' HOLOPROSENCEPHALY CHROMOSOME DELETION']",
"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:0014683",
"name": "GM50147 cell",
"definition": "[' DUPLICATED CHROMOSOME RECOMBINANT CHROMOSOME']",
"term_type": "cell line"
}
]
}