@dpavot:30535804 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/30535804","sourcedb":"@dpavot","sourceid":"30535804","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/30535804","text":"Although a digenic inheritance pattern of hearing impairment has been reported for heterozygous missense variants of ATP2B2 and CDH23, our findings indicate a monogenic cause of hearing impairment in cases with loss-of-function variants of ATP2B2.","tracks":[{"project":"PGR-UNK","denotations":[{"id":"T1","span":{"begin":117,"end":123},"obj":"493"},{"id":"T2","span":{"begin":11,"end":30},"obj":"HP:0010984"}],"relations":[{"id":"R1","pred":"unknown","subj":"T1","obj":"T2"}],"attributes":[{"subj":"T1","pred":"source","obj":"PGR-UNK"},{"subj":"T2","pred":"source","obj":"PGR-UNK"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PGR-UNK","color":"#c393ec","default":true}]}]}}