{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=23380&ordering=-name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=23340&ordering=-name","results":[{"accession":"CLO:0017455","name":"GM16659 cell","definition":"[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 RET PROTOONCOGENE; RET']","term_type":"cell line"},{"accession":"CLO:0017359","name":"GM16658 cell","definition":"[' MULTIPLE ENDOCRINE NEOPLASIA, TYPE II; MEN2 RET PROTOONCOGENE; RET']","term_type":"cell line"},{"accession":"CLO:0017363","name":"GM16654 cell","definition":"[' HUMAN VARIATION PANEL - CHINESE (VERSION 2) CHINESE POPULATION']","term_type":"cell line"},{"accession":"CLO:0017362","name":"GM16643 cell","definition":"[' FACTOR V DEFICIENCY HEMOGLOBIN--BETA LOCUS; HBB']","term_type":"cell line"},{"accession":"CLO:0017355","name":"GM16635 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG X-RAY REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 9; XRCC9']","term_type":"cell line"},{"accession":"CLO:0017354","name":"GM16634 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2']","term_type":"cell line"},{"accession":"CLO:0017357","name":"GM16633 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2']","term_type":"cell line"},{"accession":"CLO:0017356","name":"GM16632 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']","term_type":"cell line"},{"accession":"CLO:0017351","name":"GM16631 cell","definition":"[' FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA']","term_type":"cell line"},{"accession":"CLO:0017349","name":"GM16627 cell","definition":"[' NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1']","term_type":"cell line"},{"accession":"CLO:0017352","name":"GM16599 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0017405","name":"GM16598 cell","definition":"[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0017403","name":"GM16595 cell","definition":"[' CRI-DU-CHAT SYNDROME CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0017400","name":"GM16594 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0017398","name":"GM16593 cell","definition":"[' CHROMOSOME DELETION CRI-DU-CHAT SYNDROME']","term_type":"cell line"},{"accession":"CLO:0017397","name":"GM16592 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0017396","name":"GM16590 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0017395","name":"GM16589 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 5 SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0017394","name":"GM16588 cell","definition":"[' CRI-DU-CHAT SYNDROME']","term_type":"cell line"},{"accession":"CLO:0017393","name":"GM16587 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 18 SOMATIC CELL HYBRIDS']","term_type":"cell line"}]}