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- Bb0ea9651335ae9628cade7fc64d089da NCIT_P378 "NCI" @default.
- Bb0ea9651335ae9628cade7fc64d089da type Axiom @default.
- Bb0ea9651335ae9628cade7fc64d089da annotatedProperty IAO_0000115 @default.
- Bb0ea9651335ae9628cade7fc64d089da annotatedSource NCIT_C179470 @default.
- Bb0ea9651335ae9628cade7fc64d089da annotatedTarget "An inherited condition caused by mutation(s) in the NOTCH3 or PDGFRB genes, encoding neurogenic locus notch homolog protein 3 and platelet-derived growth factor receptor beta, respectively. The condition is characterized by an increased risk of developing myofibroma." @default.