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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=26540&ordering=-name",
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"results": [
{
"accession": "CLO:0023313",
"name": "GM10930 cell",
"definition": "[' FRYNS SYNDROME; FRNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023301",
"name": "GM10929 cell",
"definition": "[' ATRANSFERRINEMIA TRANSFERRIN; TF']",
"term_type": "cell line"
},
{
"accession": "CLO:0023300",
"name": "GM10927 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023299",
"name": "GM10926 cell",
"definition": "[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023327",
"name": "GM10925 cell",
"definition": "[' CHROMOSOME DELETION GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023328",
"name": "GM10924 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023329",
"name": "GM10923 cell",
"definition": "[' APPARENTLY HEALTHY NON-FETAL TISSUE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023330",
"name": "GM10922 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023324",
"name": "GM10919 cell",
"definition": "[' GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0023325",
"name": "GM10918 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023326",
"name": "GM10915 cell",
"definition": "[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE I']",
"term_type": "cell line"
},
{
"accession": "CLO:0023321",
"name": "GM10914 cell",
"definition": "[' TRANSFERRIN; TF ATRANSFERRINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023320",
"name": "GM10913 cell",
"definition": "[' ATRANSFERRINEMIA TRANSFERRIN; TF']",
"term_type": "cell line"
},
{
"accession": "CLO:0023323",
"name": "GM10912 cell",
"definition": "[' ATRANSFERRINEMIA TRANSFERRIN; TF']",
"term_type": "cell line"
},
{
"accession": "CLO:0023322",
"name": "GM10911 cell",
"definition": "[' ATRANSFERRINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023394",
"name": "GM10908 cell",
"definition": "[' CRICETULUS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023393",
"name": "GM10905 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0023396",
"name": "GM10904 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0023395",
"name": "GM10903 cell",
"definition": "[' EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE']",
"term_type": "cell line"
},
{
"accession": "CLO:0023398",
"name": "GM10902 cell",
"definition": "[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']",
"term_type": "cell line"
}
]
}