{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=23580&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=23540&ordering=-accession","results":[{"accession":"CLO:0019448","name":"GM16262 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0019447","name":"GM16260 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0019446","name":"GM16248 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0019445","name":"GM16247 cell","definition":"[' XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC']","term_type":"cell line"},{"accession":"CLO:0019444","name":"GM16245 cell","definition":"[' ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 7 SOMATIC CELL HYBRIDS CHROMOSOME 17 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0019443","name":"GM16269 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0019442","name":"GM16267 cell","definition":"[' HEMOGLOBIN--BETA LOCUS; HBB SICKLE CELL ANEMIA']","term_type":"cell line"},{"accession":"CLO:0019441","name":"GM16271 cell","definition":"[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']","term_type":"cell line"},{"accession":"CLO:0019440","name":"GM16270 cell","definition":"[' RETT SYNDROME; RTT METHYL-CPG-BINDING PROTEIN 2; MECP2']","term_type":"cell line"},{"accession":"CLO:0019439","name":"GM16266 cell","definition":"[' HEMOGLOBIN--BETA LOCUS; HBB SICKLE CELL ANEMIA']","term_type":"cell line"},{"accession":"CLO:0019438","name":"GM16265 cell","definition":"[' SICKLE CELL ANEMIA HEMOGLOBIN--BETA LOCUS; HBB']","term_type":"cell line"},{"accession":"CLO:0019437","name":"GM12268 cell","definition":"[' CEPH/UTAH PEDIGREE 1418']","term_type":"cell line"},{"accession":"CLO:0019436","name":"GM12267 cell","definition":"[' CEPH/UTAH PEDIGREE 1418']","term_type":"cell line"},{"accession":"CLO:0019435","name":"GM12266 cell","definition":"[' CEPH/UTAH PEDIGREE 1418']","term_type":"cell line"},{"accession":"CLO:0019434","name":"GM12265 cell","definition":"[' CEPH/UTAH PEDIGREE 1418']","term_type":"cell line"},{"accession":"CLO:0019433","name":"GM16347 cell","definition":"[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN  (FSHD)']","term_type":"cell line"},{"accession":"CLO:0019432","name":"GM12272 cell","definition":"[' CEPH/UTAH PEDIGREE 1418 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE II) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]']","term_type":"cell line"},{"accession":"CLO:0019431","name":"GM16272 cell","definition":"[' NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3']","term_type":"cell line"},{"accession":"CLO:0019430","name":"GM12271 cell","definition":"[' CEPH/UTAH PEDIGREE 1418']","term_type":"cell line"},{"accession":"CLO:0019429","name":"GM16349 cell","definition":"[' FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; TYPE UNKNOWN  (FSHD) TURNER SYNDROME']","term_type":"cell line"}]}