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- B0bd8db11d3af9977072a53219ff33d89 NCIT_P378 "NCI" @default.
- B0bd8db11d3af9977072a53219ff33d89 type Axiom @default.
- B0bd8db11d3af9977072a53219ff33d89 annotatedProperty IAO_0000115 @default.
- B0bd8db11d3af9977072a53219ff33d89 annotatedSource NCIT_C4705 @default.
- B0bd8db11d3af9977072a53219ff33d89 annotatedTarget "An autosomal dominant disorder most often caused by mutations in the PRKAR1A gene. It is characterized by the presence of myxomas in the heart and skin, skin hyperpigmentation, increased endocrine activity and melanotic schwannomas." @default.