{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=37700&ordering=accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=37660&ordering=accession","results":[{"accession":"CLO:0036892","name":"GM07152 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036893","name":"AG01440 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0036894","name":"AG01178 cell","definition":"[' HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS']","term_type":"cell line"},{"accession":"CLO:0036895","name":"GM07157 cell","definition":"[' PELIZAEUS-MERZBACHER DISEASE; PMD']","term_type":"cell line"},{"accession":"CLO:0036896","name":"GM07158 cell","definition":"[' TRANSLOCATED CHROMOSOME FUMARATE HYDRATASE; FH']","term_type":"cell line"},{"accession":"CLO:0036897","name":"AG01437 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0036898","name":"GM07155 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036899","name":"AG00990 cell","definition":"[' SEIP SYNDROME LAMIN A/C; LMNA']","term_type":"cell line"},{"accession":"CLO:0036900","name":"GM07156 cell","definition":"[' PELIZAEUS-MERZBACHER DISEASE; PMD']","term_type":"cell line"},{"accession":"CLO:0036901","name":"GM07166 cell","definition":"[' NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 NIJMEGEN BREAKAGE SYNDROME']","term_type":"cell line"},{"accession":"CLO:0036902","name":"AG01522 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0036903","name":"AG01520 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0036904","name":"AG01521 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0036905","name":"GM07173 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0036906","name":"GM07172 cell","definition":"[' EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE']","term_type":"cell line"},{"accession":"CLO:0036907","name":"GM07200 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036908","name":"GM07201 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036909","name":"GM07205 cell","definition":"[' MAJOR AFFECTIVE DISORDER - 125480 OR 309200']","term_type":"cell line"},{"accession":"CLO:0036910","name":"GM07206 cell","definition":"[' EHLERS-DANLOS SYNDROME, TYPE VI']","term_type":"cell line"},{"accession":"CLO:0036911","name":"GM07174 cell","definition":"[' FRAGILE SITE MENTAL RETARDATION 1; FMR1']","term_type":"cell line"}]}