{"count":43797,"next":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=12040&ordering=-accession","previous":"https://cinder.proteo.info/api/ms_vocab/?format=json&limit=20&offset=12000&ordering=-accession","results":[{"accession":"CLO:0030988","name":"GM01712 cell","definition":"[' COCKAYNE SYNDROME TYPE I - 216400 OR TYPE III - 216411']","term_type":"cell line"},{"accession":"CLO:0030987","name":"GM01715 cell","definition":"[' ADENOSINE DEAMINASE; ADA 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:0030986","name":"GM01720 cell","definition":"[' NEURAMINIDASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0030985","name":"GM01719 cell","definition":"[' NEURAMINIDASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0030984","name":"GM01718 cell","definition":"[' NEURAMINIDASE DEFICIENCY']","term_type":"cell line"},{"accession":"CLO:0030983","name":"GM01717 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0030982","name":"GM01726 cell","definition":"[' BASAL CELL NEVUS SYNDROME; BCNS']","term_type":"cell line"},{"accession":"CLO:0030981","name":"GM01725 cell","definition":"[' BASAL CELL NEVUS SYNDROME; BCNS']","term_type":"cell line"},{"accession":"CLO:0030980","name":"GM01723 cell","definition":"[' ANEUPLOID CHROMOSOME NUMBER - NON-TRISOMIC']","term_type":"cell line"},{"accession":"CLO:0030979","name":"GM01721 cell","definition":"[' ANDROGEN RECEPTOR; AR']","term_type":"cell line"},{"accession":"CLO:0030978","name":"GM01696 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0030977","name":"GM01704 cell","definition":"[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']","term_type":"cell line"},{"accession":"CLO:0030976","name":"GM01706 cell","definition":"[' APPARENTLY HEALTHY NON-FETAL TISSUE']","term_type":"cell line"},{"accession":"CLO:0030975","name":"GM01707 cell","definition":"[' CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR CYSTIC FIBROSIS; CF']","term_type":"cell line"},{"accession":"CLO:0030974","name":"GM01708 cell","definition":"[' CYSTIC FIBROSIS; CF']","term_type":"cell line"},{"accession":"CLO:0030973","name":"GM01700 cell","definition":"[' TRANSLOCATED CHROMOSOME']","term_type":"cell line"},{"accession":"CLO:0030972","name":"GM01701 cell","definition":"[' WOLFRAM SYNDROME']","term_type":"cell line"},{"accession":"CLO:0030971","name":"GM01702 cell","definition":"[' GLYCOGEN STORAGE DISEASE VIII (IX, INCLUDED)']","term_type":"cell line"},{"accession":"CLO:0030970","name":"GM01703 cell","definition":"[' GALACTOSEMIA GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; GALT']","term_type":"cell line"},{"accession":"CLO:0030969","name":"GM01709 cell","definition":"[' DICENTRIC CHROMOSOME GONADAL DYSGENESIS']","term_type":"cell line"}]}