{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=26540&ordering=-name","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=26500&ordering=-name","results":[{"accession":"CLO:0023313","name":"GM10930 cell","definition":"[' FRYNS SYNDROME; FRNS']","term_type":"cell line"},{"accession":"CLO:0023301","name":"GM10929 cell","definition":"[' ATRANSFERRINEMIA TRANSFERRIN; TF']","term_type":"cell line"},{"accession":"CLO:0023300","name":"GM10927 cell","definition":"[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0023299","name":"GM10926 cell","definition":"[' NIGMS MAPPING PANEL #2, VERSION 3, HUMAN/RODENT SOMATIC CELL HYBRIDS']","term_type":"cell line"},{"accession":"CLO:0023327","name":"GM10925 cell","definition":"[' CHROMOSOME DELETION GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS']","term_type":"cell line"},{"accession":"CLO:0023328","name":"GM10924 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0023329","name":"GM10923 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0023330","name":"GM10922 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0023324","name":"GM10919 cell","definition":"[' GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I']","term_type":"cell line"},{"accession":"CLO:0023325","name":"GM10918 cell","definition":"[' CHROMOSOME DELETION']","term_type":"cell line"},{"accession":"CLO:0023326","name":"GM10915 cell","definition":"[' GLUCOSIDASE, ACID BETA; GBA GAUCHER DISEASE, TYPE I']","term_type":"cell line"},{"accession":"CLO:0023321","name":"GM10914 cell","definition":"[' TRANSFERRIN; TF ATRANSFERRINEMIA']","term_type":"cell line"},{"accession":"CLO:0023320","name":"GM10913 cell","definition":"[' ATRANSFERRINEMIA TRANSFERRIN; TF']","term_type":"cell line"},{"accession":"CLO:0023323","name":"GM10912 cell","definition":"[' ATRANSFERRINEMIA TRANSFERRIN; TF']","term_type":"cell line"},{"accession":"CLO:0023322","name":"GM10911 cell","definition":"[' ATRANSFERRINEMIA']","term_type":"cell line"},{"accession":"CLO:0023394","name":"GM10908 cell","definition":"[' CRICETULUS']","term_type":"cell line"},{"accession":"CLO:0023393","name":"GM10905 cell","definition":"[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']","term_type":"cell line"},{"accession":"CLO:0023396","name":"GM10904 cell","definition":"[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']","term_type":"cell line"},{"accession":"CLO:0023395","name":"GM10903 cell","definition":"[' EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE']","term_type":"cell line"},{"accession":"CLO:0023398","name":"GM10902 cell","definition":"[' XERODERMIC IDIOCY OF DE SANCTIS AND CACCHIONE EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 6; ERCC6 COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED']","term_type":"cell line"}]}