CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 427861-428064 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T51705","span":{"begin":0,"end":203},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Of roughly 5000 patients with a pathogenic variant, 2.9% had single-exon CNVs,1.8% a large indel or complex sequence change, and 5.8% a variant in a region of high-GC, low complexity or poor mappability."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T144","span":{"begin":0,"end":203},"obj":"Sentence"}],"text":"Of roughly 5000 patients with a pathogenic variant, 2.9% had single-exon CNVs,1.8% a large indel or complex sequence change, and 5.8% a variant in a region of high-GC, low complexity or poor mappability."}