CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 100007-100209 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/CORD-19/sourceid/ee0a7632371a08727d41e55aad7d621daeceef7d","sourcedb":"CORD-19","sourceid":"ee0a7632371a08727d41e55aad7d621daeceef7d","text":"Here, we hypothesize that implementation of a genome-wide SNP sequencing backbone will allow for sensitive and comprehensive detection of genome-wide CNVs and CN-LOH by NGS for hematologic malignancies.","tracks":[{"project":"CORD-19-Sentences","denotations":[{"id":"T34861","span":{"begin":0,"end":202},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T34861","pred":"source","obj":"CORD-19-Sentences"}]},{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T103","span":{"begin":0,"end":202},"obj":"Sentence"}],"attributes":[{"subj":"T103","pred":"source","obj":"CORD-19_Custom_license_subset"}]},{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T549","span":{"begin":177,"end":201},"obj":"Disease"},{"id":"T548","span":{"begin":177,"end":201},"obj":"Disease"}],"attributes":[{"id":"A549","pred":"mondo_id","subj":"T549","obj":"http://purl.obolibrary.org/obo/MONDO_0002334"},{"id":"A550","pred":"mondo_id","subj":"T549","obj":"http://purl.obolibrary.org/obo/MONDO_0044881"},{"id":"A92678","pred":"mondo_id","subj":"T548","obj":"http://purl.obolibrary.org/obo/MONDO_0002334"},{"id":"A67028","pred":"mondo_id","subj":"T548","obj":"http://purl.obolibrary.org/obo/MONDO_0044881"},{"subj":"T549","pred":"source","obj":"CORD-19-PD-MONDO"},{"subj":"T548","pred":"source","obj":"CORD-19-PD-MONDO"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"CORD-19-Sentences","color":"#93a7ec","default":true},{"id":"CORD-19_Custom_license_subset","color":"#c1ec93"},{"id":"CORD-19-PD-MONDO","color":"#ec93db"}]}]}}