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- Bf0d0fea6035542ed3aab4e850f937f47 NCIT_P378 "NCI" @default.
- Bf0d0fea6035542ed3aab4e850f937f47 type Axiom @default.
- Bf0d0fea6035542ed3aab4e850f937f47 annotatedProperty IAO_0000115 @default.
- Bf0d0fea6035542ed3aab4e850f937f47 annotatedSource NCIT_C96816 @default.
- Bf0d0fea6035542ed3aab4e850f937f47 annotatedTarget "A role used to assert a direct relationship between a disease, disorder or finding and a gene. This restriction can be used when a polymorphism or an abnormality in a gene is either a clinical marker for, a causative event for, or predisposes a subject to a disease. The domain and range for this role are 'Disease, Disorder or Finding' and 'Gene', respectively." @default.