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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=24120&ordering=accession",
"previous": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=24080&ordering=accession",
"results": [
{
"accession": "CLO:0023312",
"name": "GM10931 cell",
"definition": "[' FRYNS SYNDROME; FRNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023313",
"name": "GM10930 cell",
"definition": "[' FRYNS SYNDROME; FRNS']",
"term_type": "cell line"
},
{
"accession": "CLO:0023314",
"name": "GM10933 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023315",
"name": "GM10932 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
},
{
"accession": "CLO:0023316",
"name": "GM10935 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023317",
"name": "GM10934 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023318",
"name": "GM10947 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023319",
"name": "GM10946 cell",
"definition": "[' OCULAR ALBINISM WITH CHROMOSOME ABNORMALITY; POSSIBLE AUTO RECESSIVE INHERITANCE MARKER CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0023320",
"name": "GM10913 cell",
"definition": "[' ATRANSFERRINEMIA TRANSFERRIN; TF']",
"term_type": "cell line"
},
{
"accession": "CLO:0023321",
"name": "GM10914 cell",
"definition": "[' TRANSFERRIN; TF ATRANSFERRINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023322",
"name": "GM10911 cell",
"definition": "[' ATRANSFERRINEMIA']",
"term_type": "cell line"
},
{
"accession": "CLO:0023323",
"name": "GM10912 cell",
"definition": "[' ATRANSFERRINEMIA TRANSFERRIN; TF']",
"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: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:0023331",
"name": "GM10967 cell",
"definition": "[' AMERINDIAN POPULATION']",
"term_type": "cell line"
}
]
}