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{
"count": 43797,
"next": "https://cinder.proteo.info/api/ms_vocab/?format=api&limit=20&offset=27000&ordering=-accession",
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{
"accession": "CLO:0016028",
"name": "GM03870 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016027",
"name": "GM17983 cell",
"definition": "[' INTERNATIONAL HAPMAP PROJECT - HAN CHINESE IN METROPOLITAN DENVER, COLORADO INTERNATIONAL HAPMAP PROJECT - PANEL OF 90 HAN CHINESE IN METROPOLITAN DENVER, COLORADO']",
"term_type": "cell line"
},
{
"accession": "CLO:0016026",
"name": "GM03869 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016025",
"name": "GM03868 cell",
"definition": "[' HUNTINGTON DISEASE; HD']",
"term_type": "cell line"
},
{
"accession": "CLO:0016024",
"name": "GM18016 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016023",
"name": "GM03893 cell",
"definition": "[' RETINITIS PIGMENTOSA - 180100, 268000, OR 312600']",
"term_type": "cell line"
},
{
"accession": "CLO:0016022",
"name": "GM03892 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016021",
"name": "GM18015 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016020",
"name": "GM18018 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016019",
"name": "GM18017 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016018",
"name": "GM03894 cell",
"definition": "[' RETINITIS PIGMENTOSA - 180100, 268000, OR 312600']",
"term_type": "cell line"
},
{
"accession": "CLO:0016017",
"name": "GM18012 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016016",
"name": "GM18011 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016015",
"name": "GM18014 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016014",
"name": "GM18013 cell",
"definition": "[' HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 200 HUMAN VARIATION PANEL - CAUCASIAN PANEL OF 100 (SET 2)']",
"term_type": "cell line"
},
{
"accession": "CLO:0016013",
"name": "GM03883 cell",
"definition": "[' INVERTED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016012",
"name": "GM03886 cell",
"definition": "[' TRANSLOCATED CHROMOSOME']",
"term_type": "cell line"
},
{
"accession": "CLO:0016011",
"name": "GM03884 cell",
"definition": "[' TRANSLOCATED CHROMOSOME KLIPPEL-FEIL SYNDROME; KFS; KFM CERVICAL VERTEBRAL FUSION, TYPE II, INCLUDED']",
"term_type": "cell line"
},
{
"accession": "CLO:0016010",
"name": "GM03889 cell",
"definition": "[' USHER SYNDROME, TYPE IA; USH1A']",
"term_type": "cell line"
},
{
"accession": "CLO:0016009",
"name": "GM03887 cell",
"definition": "[' CHROMOSOME DELETION']",
"term_type": "cell line"
}
]
}