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- B311063be084848d324d0e2cba28f14fc NCIT_P378 "NCI" @default.
- B311063be084848d324d0e2cba28f14fc type Axiom @default.
- B311063be084848d324d0e2cba28f14fc annotatedProperty IAO_0000115 @default.
- B311063be084848d324d0e2cba28f14fc annotatedSource NCIT_C75480 @default.
- B311063be084848d324d0e2cba28f14fc annotatedTarget "The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3." @default.