{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=37600&ordering=accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=37560&ordering=accession","results":[{"accession":"CLO:0036792","name":"GM07071 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036793","name":"GM07063 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036794","name":"GM07062 cell","definition":"[' CEPH/UTAH PEDIGREE 1340']","term_type":"cell line"},{"accession":"CLO:0036795","name":"GM07065 cell","definition":"[' ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE']","term_type":"cell line"},{"accession":"CLO:0036796","name":"GM07064 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"},{"accession":"CLO:0036797","name":"GM07059 cell","definition":"[' CEPH/UTAH PEDIGREE 1331']","term_type":"cell line"},{"accession":"CLO:0036798","name":"GM07060 cell","definition":"[' CEPH/UTAH PEDIGREE 13293']","term_type":"cell line"},{"accession":"CLO:0036799","name":"GM07058 cell","definition":"[' CEPH/UTAH PEDIGREE 13291']","term_type":"cell line"},{"accession":"CLO:0036800","name":"GM07057 cell","definition":"[' SNP500 PANEL CEPH/UTAH PEDIGREE 1331']","term_type":"cell line"},{"accession":"CLO:0036801","name":"GM07056 cell","definition":"[' CEPH/UTAH PEDIGREE 1340 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE] CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19']","term_type":"cell line"},{"accession":"CLO:0036802","name":"GM07055 cell","definition":"[' CEPH/UTAH PEDIGREE 1341 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE] CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19']","term_type":"cell line"},{"accession":"CLO:0036803","name":"GM07054 cell","definition":"[' CEPH/UTAH PEDIGREE 13294']","term_type":"cell line"},{"accession":"CLO:0036804","name":"GM07053 cell","definition":"[' CEPH/UTAH PEDIGREE 1340']","term_type":"cell line"},{"accession":"CLO:0036805","name":"GM07052 cell","definition":"[' CEPH/UTAH PEDIGREE 1333']","term_type":"cell line"},{"accession":"CLO:0036806","name":"GM07051 cell","definition":"[' CEPH/UTAH PEDIGREE 13292 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE II) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]']","term_type":"cell line"},{"accession":"CLO:0036807","name":"GM07050 cell","definition":"[' CEPH/UTAH PEDIGREE 1331']","term_type":"cell line"},{"accession":"CLO:0036808","name":"GM07048 cell","definition":"[' INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE] CEPH/UTAH PEDIGREE 1341 CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19']","term_type":"cell line"},{"accession":"CLO:0036809","name":"GM07049 cell","definition":"[' CEPH/UTAH PEDIGREE 1333']","term_type":"cell line"},{"accession":"CLO:0036810","name":"GM07104 cell","definition":"[' SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0036811","name":"GM07114 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"}]}