@dpavot:26680691 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/26680691","sourcedb":"@dpavot","sourceid":"26680691","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/26680691","text":"CGD is a genetically heterogeneous disease with an X-linked recessive (XR-CGD) form caused by mutations in the CYBB gene encoding the gp91(phox) protein, and an autosomal recessive (AR-CGD) form caused by mutations in the CYBA, NCF1, NCF2, or NCF4 genes encoding p22(phox) , p47(phox) , p67(phox) , and p40(phox) , respectively.","tracks":[{"project":"PGR-UNK","denotations":[{"id":"T1","span":{"begin":222,"end":226},"obj":"1535"},{"id":"T2","span":{"begin":21,"end":34},"obj":"HP:0001425"}],"relations":[{"id":"R1","pred":"unknown ","subj":"T2","obj":"T1"}],"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":"#93ec9a","default":true}]}]}}