PMC:7274950 / 1483-1629 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T16","span":{"begin":53,"end":54},"obj":"GO:0000805"},{"id":"T17","span":{"begin":72,"end":81},"obj":"GO:0005764"},{"id":"T41907","span":{"begin":53,"end":54},"obj":"GO:0000805"},{"id":"T48067","span":{"begin":72,"end":81},"obj":"GO:0005764"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PubTator","denotations":[{"id":"43","span":{"begin":0,"end":13},"obj":"Disease"},{"id":"58","span":{"begin":16,"end":29},"obj":"Disease"},{"id":"59","span":{"begin":31,"end":33},"obj":"Disease"},{"id":"60","span":{"begin":53,"end":98},"obj":"Disease"}],"attributes":[{"id":"A43","pred":"tao:has_database_id","subj":"43","obj":"MESH:D000795"},{"id":"A58","pred":"tao:has_database_id","subj":"58","obj":"MESH:D000795"},{"id":"A59","pred":"tao:has_database_id","subj":"59","obj":"MESH:D004402"},{"id":"A60","pred":"tao:has_database_id","subj":"60","obj":"MESH:D016464"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T4","span":{"begin":72,"end":81},"obj":"Body_part"}],"attributes":[{"id":"A4","pred":"fma_id","subj":"T4","obj":"http://purl.org/sig/ont/fma/fma63836"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PD-MONDO","denotations":[{"id":"T16","span":{"begin":0,"end":13},"obj":"Disease"},{"id":"T17","span":{"begin":16,"end":29},"obj":"Disease"},{"id":"T18","span":{"begin":31,"end":33},"obj":"Disease"},{"id":"T19","span":{"begin":72,"end":98},"obj":"Disease"}],"attributes":[{"id":"A16","pred":"mondo_id","subj":"T16","obj":"http://purl.obolibrary.org/obo/MONDO_0010526"},{"id":"A17","pred":"mondo_id","subj":"T17","obj":"http://purl.obolibrary.org/obo/MONDO_0010526"},{"id":"A18","pred":"mondo_id","subj":"T18","obj":"http://purl.obolibrary.org/obo/MONDO_0010526"},{"id":"A19","pred":"mondo_id","subj":"T19","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T12","span":{"begin":38,"end":39},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T13","span":{"begin":72,"end":81},"obj":"http://purl.obolibrary.org/obo/GO_0005764"},{"id":"T14","span":{"begin":142,"end":143},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T2","span":{"begin":31,"end":33},"obj":"Chemical"}],"attributes":[{"id":"A2","pred":"chebi_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CHEBI_73631"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}

{"project":"LitCovid-PD-GO-BP","denotations":[{"id":"T2","span":{"begin":82,"end":89},"obj":"http://purl.obolibrary.org/obo/GO_0051235"}],"text":"Fabry disease.\n\nFabry disease (FD) is a progressive, X-linked inherited lysosomal storage disorder caused by mutations in the α-Galactosidase A ge"}