CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 521553-521721 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T39172","span":{"begin":0,"end":168},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Since patients with SFT in the liver are rare, a comprehensive genetic analysis offers clinical evidence and directions for further research of the pathogenesis of SFT."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T214","span":{"begin":0,"end":168},"obj":"Sentence"}],"text":"Since patients with SFT in the liver are rare, a comprehensive genetic analysis offers clinical evidence and directions for further research of the pathogenesis of SFT."}

{"project":"CORD-19-PD-UBERON","denotations":[{"id":"T428","span":{"begin":31,"end":36},"obj":"Body_part"}],"attributes":[{"id":"A428","pred":"uberon_id","subj":"T428","obj":"http://purl.obolibrary.org/obo/UBERON_0002107"}],"text":"Since patients with SFT in the liver are rare, a comprehensive genetic analysis offers clinical evidence and directions for further research of the pathogenesis of SFT."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T2485","span":{"begin":20,"end":23},"obj":"Disease"},{"id":"T2486","span":{"begin":164,"end":167},"obj":"Disease"},{"id":"T57902","span":{"begin":20,"end":23},"obj":"Disease"},{"id":"T4848","span":{"begin":164,"end":167},"obj":"Disease"}],"attributes":[{"id":"A2485","pred":"mondo_id","subj":"T2485","obj":"http://purl.obolibrary.org/obo/MONDO_0016238"},{"id":"A2486","pred":"mondo_id","subj":"T2486","obj":"http://purl.obolibrary.org/obo/MONDO_0016238"},{"id":"A9589","pred":"mondo_id","subj":"T57902","obj":"http://purl.obolibrary.org/obo/MONDO_0016238"},{"id":"A19072","pred":"mondo_id","subj":"T4848","obj":"http://purl.obolibrary.org/obo/MONDO_0016238"}],"text":"Since patients with SFT in the liver are rare, a comprehensive genetic analysis offers clinical evidence and directions for further research of the pathogenesis of SFT."}