CORD-19:932bcdd2f6c6d487386e8bf983e4874387771be1 / 123970-124214 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T8808","span":{"begin":0,"end":244},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}

{"project":"Epistemic_Statements","denotations":[{"id":"T281","span":{"begin":0,"end":244},"obj":"Epistemic_statement"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T253","span":{"begin":0,"end":244},"obj":"Sentence"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}

{"project":"CORD-19-PD-HP","denotations":[{"id":"T210","span":{"begin":19,"end":35},"obj":"Phenotype"},{"id":"T211","span":{"begin":155,"end":171},"obj":"Phenotype"}],"attributes":[{"id":"A210","pred":"hp_id","subj":"T210","obj":"http://purl.obolibrary.org/obo/HP_0001138"},{"id":"A211","pred":"hp_id","subj":"T211","obj":"http://purl.obolibrary.org/obo/HP_0001138"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}

{"project":"CORD-19-PD-UBERON","denotations":[{"id":"T328","span":{"begin":223,"end":235},"obj":"Body_part"}],"attributes":[{"id":"A328","pred":"uberon_id","subj":"T328","obj":"http://purl.obolibrary.org/obo/UBERON_0002316"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T605","span":{"begin":0,"end":35},"obj":"Disease"},{"id":"T606","span":{"begin":8,"end":35},"obj":"Disease"},{"id":"T607","span":{"begin":19,"end":35},"obj":"Disease"},{"id":"T608","span":{"begin":25,"end":35},"obj":"Disease"},{"id":"T609","span":{"begin":37,"end":41},"obj":"Disease"},{"id":"T610","span":{"begin":155,"end":171},"obj":"Disease"},{"id":"T611","span":{"begin":161,"end":171},"obj":"Disease"},{"id":"T612","span":{"begin":195,"end":213},"obj":"Disease"},{"id":"T613","span":{"begin":215,"end":217},"obj":"Disease"},{"id":"T80390","span":{"begin":0,"end":35},"obj":"Disease"},{"id":"T8929","span":{"begin":8,"end":35},"obj":"Disease"},{"id":"T21837","span":{"begin":19,"end":35},"obj":"Disease"},{"id":"T96696","span":{"begin":25,"end":35},"obj":"Disease"},{"id":"T41433","span":{"begin":37,"end":41},"obj":"Disease"},{"id":"T77298","span":{"begin":155,"end":171},"obj":"Disease"},{"id":"T35119","span":{"begin":161,"end":171},"obj":"Disease"},{"id":"T48102","span":{"begin":195,"end":213},"obj":"Disease"},{"id":"T48718","span":{"begin":215,"end":217},"obj":"Disease"}],"attributes":[{"id":"A605","pred":"mondo_id","subj":"T605","obj":"http://purl.obolibrary.org/obo/MONDO_0010788"},{"id":"A606","pred":"mondo_id","subj":"T606","obj":"http://purl.obolibrary.org/obo/MONDO_0020249"},{"id":"A607","pred":"mondo_id","subj":"T607","obj":"http://purl.obolibrary.org/obo/MONDO_0002135"},{"id":"A608","pred":"mondo_id","subj":"T608","obj":"http://purl.obolibrary.org/obo/MONDO_0005244"},{"id":"A609","pred":"mondo_id","subj":"T609","obj":"http://purl.obolibrary.org/obo/MONDO_0010788"},{"id":"A610","pred":"mondo_id","subj":"T610","obj":"http://purl.obolibrary.org/obo/MONDO_0002135"},{"id":"A611","pred":"mondo_id","subj":"T611","obj":"http://purl.obolibrary.org/obo/MONDO_0005244"},{"id":"A612","pred":"mondo_id","subj":"T612","obj":"http://purl.obolibrary.org/obo/MONDO_0005301"},{"id":"A613","pred":"mondo_id","subj":"T613","obj":"http://purl.obolibrary.org/obo/MONDO_0005301"},{"id":"A34304","pred":"mondo_id","subj":"T80390","obj":"http://purl.obolibrary.org/obo/MONDO_0010788"},{"id":"A94450","pred":"mondo_id","subj":"T8929","obj":"http://purl.obolibrary.org/obo/MONDO_0020249"},{"id":"A39099","pred":"mondo_id","subj":"T21837","obj":"http://purl.obolibrary.org/obo/MONDO_0002135"},{"id":"A55970","pred":"mondo_id","subj":"T96696","obj":"http://purl.obolibrary.org/obo/MONDO_0005244"},{"id":"A92577","pred":"mondo_id","subj":"T41433","obj":"http://purl.obolibrary.org/obo/MONDO_0010788"},{"id":"A17729","pred":"mondo_id","subj":"T77298","obj":"http://purl.obolibrary.org/obo/MONDO_0002135"},{"id":"A49798","pred":"mondo_id","subj":"T35119","obj":"http://purl.obolibrary.org/obo/MONDO_0005244"},{"id":"A27991","pred":"mondo_id","subj":"T48102","obj":"http://purl.obolibrary.org/obo/MONDO_0005301"},{"id":"A93630","pred":"mondo_id","subj":"T48718","obj":"http://purl.obolibrary.org/obo/MONDO_0005301"}],"text":"Leber's hereditary optic neuropathy (LHON) is associated with point mutations in the mitochondrial DNA and characterized by bilateral, usually sequential, optic neuropathy that may co-occur with multiple sclerosis (MS)like white matter lesions."}