PubMed:11087738 / 182-318 JSONTXT

{"project":"sentences","denotations":[{"id":"T2","span":{"begin":0,"end":136},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Gerstmann-Sträussler-Scheinker disease (GSS) is a cerebral amyloidosis associated with mutations in the prion protein (PrP) gene (PRNP)."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":59,"end":70},"obj":"HP:0011034"}],"text":"Gerstmann-Sträussler-Scheinker disease (GSS) is a cerebral amyloidosis associated with mutations in the prion protein (PrP) gene (PRNP)."}

{"project":"mondo_disease","denotations":[{"id":"T3","span":{"begin":0,"end":38},"obj":"Disease"},{"id":"T4","span":{"begin":40,"end":43},"obj":"Disease"},{"id":"T5","span":{"begin":59,"end":70},"obj":"Disease"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0007656"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0007656"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MONDO_0019065"}],"text":"Gerstmann-Sträussler-Scheinker disease (GSS) is a cerebral amyloidosis associated with mutations in the prion protein (PrP) gene (PRNP)."}

{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":59,"end":70},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0011034"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Gerstmann-Sträussler-Scheinker disease (GSS) is a cerebral amyloidosis associated with mutations in the prion protein (PrP) gene (PRNP)."}