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- B159bafbf33abffe1b69c31a266b5f3bc NCIT_P378 "NCI" @default.
- B159bafbf33abffe1b69c31a266b5f3bc type Axiom @default.
- B159bafbf33abffe1b69c31a266b5f3bc annotatedProperty IAO_0000115 @default.
- B159bafbf33abffe1b69c31a266b5f3bc annotatedSource NCIT_C118636 @default.
- B159bafbf33abffe1b69c31a266b5f3bc annotatedTarget "A rare, autosomal dominant inherited syndrome caused by mutations in the FBN1 gene. It is characterized by hard and thickened skin, usually over the entire body, and limited joint motility." @default.