CORD-19:02d18b4f484a0420c21595a95b8765125d4a484c / 41028-41217 JSONTXT

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T232","span":{"begin":0,"end":189},"obj":"Sentence"}],"text":"Hartnup disorder is a hereditary familial disease, characterized by a pellagra-like light-sensitive rash, cerebellar ataxia, emotional instability, and amino aciduria (Baron et al., 1956) ."}

{"project":"CORD-19-Sentences","denotations":[{"id":"TextSentencer_T232","span":{"begin":0,"end":189},"obj":"Sentence"},{"id":"TextSentencer_T232","span":{"begin":0,"end":189},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Hartnup disorder is a hereditary familial disease, characterized by a pellagra-like light-sensitive rash, cerebellar ataxia, emotional instability, and amino aciduria (Baron et al., 1956) ."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T265","span":{"begin":0,"end":16},"obj":"Disease"},{"id":"T266","span":{"begin":70,"end":78},"obj":"Disease"},{"id":"T267","span":{"begin":106,"end":123},"obj":"Disease"}],"attributes":[{"id":"A265","pred":"mondo_id","subj":"T265","obj":"http://purl.obolibrary.org/obo/MONDO_0009324"},{"id":"A266","pred":"mondo_id","subj":"T266","obj":"http://purl.obolibrary.org/obo/MONDO_0019975"},{"id":"A267","pred":"mondo_id","subj":"T267","obj":"http://purl.obolibrary.org/obo/MONDO_0000437"}],"text":"Hartnup disorder is a hereditary familial disease, characterized by a pellagra-like light-sensitive rash, cerebellar ataxia, emotional instability, and amino aciduria (Baron et al., 1956) ."}

{"project":"CORD-19-PD-HP","denotations":[{"id":"T61","span":{"begin":100,"end":104},"obj":"Phenotype"},{"id":"T62","span":{"begin":106,"end":123},"obj":"Phenotype"},{"id":"T63","span":{"begin":125,"end":146},"obj":"Phenotype"},{"id":"T64","span":{"begin":152,"end":166},"obj":"Phenotype"},{"id":"T65","span":{"begin":158,"end":166},"obj":"Phenotype"}],"attributes":[{"id":"A61","pred":"hp_id","subj":"T61","obj":"http://purl.obolibrary.org/obo/HP_0000988"},{"id":"A62","pred":"hp_id","subj":"T62","obj":"http://purl.obolibrary.org/obo/HP_0001251"},{"id":"A63","pred":"hp_id","subj":"T63","obj":"http://purl.obolibrary.org/obo/HP_0000712"},{"id":"A64","pred":"hp_id","subj":"T64","obj":"http://purl.obolibrary.org/obo/HP_0003355"},{"id":"A65","pred":"hp_id","subj":"T65","obj":"http://purl.obolibrary.org/obo/HP_0012072"}],"text":"Hartnup disorder is a hereditary familial disease, characterized by a pellagra-like light-sensitive rash, cerebellar ataxia, emotional instability, and amino aciduria (Baron et al., 1956) ."}