PMC:7274950 / 140-370 JSONTXT

{"project":"LitCovid-PMC-OGER-BB","denotations":[{"id":"T3","span":{"begin":20,"end":29},"obj":"GO:0005764"},{"id":"T4","span":{"begin":210,"end":217},"obj":"UBERON:0000948"},{"id":"T5","span":{"begin":219,"end":227},"obj":"UBERON:0001893"},{"id":"T12628","span":{"begin":20,"end":29},"obj":"GO:0005764"},{"id":"T151","span":{"begin":210,"end":217},"obj":"UBERON:0000948"},{"id":"T63646","span":{"begin":219,"end":227},"obj":"UBERON:0001893"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PubTator","denotations":[{"id":"28","span":{"begin":116,"end":131},"obj":"Disease"},{"id":"29","span":{"begin":133,"end":161},"obj":"Disease"}],"attributes":[{"id":"A28","pred":"tao:has_database_id","subj":"28","obj":"MESH:D010292"},{"id":"A29","pred":"tao:has_database_id","subj":"29","obj":"MESH:D000794"}],"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":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PD-FMA-UBERON","denotations":[{"id":"T1","span":{"begin":20,"end":29},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"fma_id","subj":"T1","obj":"http://purl.org/sig/ont/fma/fma63836"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PD-MONDO","denotations":[{"id":"T5","span":{"begin":148,"end":161},"obj":"Disease"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MONDO_0003143"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PD-CLO","denotations":[{"id":"T1","span":{"begin":0,"end":1},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T2","span":{"begin":20,"end":29},"obj":"http://purl.obolibrary.org/obo/GO_0005764"},{"id":"T3","span":{"begin":57,"end":58},"obj":"http://purl.obolibrary.org/obo/CLO_0001020"},{"id":"T4","span":{"begin":102,"end":107},"obj":"http://purl.obolibrary.org/obo/UBERON_0003101"},{"id":"T5","span":{"begin":102,"end":107},"obj":"http://www.ebi.ac.uk/efo/EFO_0000970"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PD-CHEBI","denotations":[{"id":"T1","span":{"begin":37,"end":42},"obj":"Chemical"}],"attributes":[{"id":"A1","pred":"chebi_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CHEBI_30216"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}

{"project":"LitCovid-PD-HP","denotations":[{"id":"T1","span":{"begin":116,"end":131},"obj":"Phenotype"},{"id":"T2","span":{"begin":133,"end":143},"obj":"Phenotype"},{"id":"T3","span":{"begin":148,"end":161},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/HP_0031006"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/HP_0000970"},{"id":"A3","pred":"hp_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/HP_0001014"}],"text":"a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral an"}