@dpavot:26680691 JSONTXT

{"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"}],"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."}