Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B719a5ea2b7305c93dcac1b51a8e9f3bc> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B719a5ea2b7305c93dcac1b51a8e9f3bc NCIT_P378 "NCI" @default.
- B719a5ea2b7305c93dcac1b51a8e9f3bc type Axiom @default.
- B719a5ea2b7305c93dcac1b51a8e9f3bc annotatedProperty IAO_0000115 @default.
- B719a5ea2b7305c93dcac1b51a8e9f3bc annotatedSource NCIT_C176943 @default.
- B719a5ea2b7305c93dcac1b51a8e9f3bc annotatedTarget "A rare inherited form of myofibromatosis caused by autosomal dominant mutation(s) in the PDGFRB gene, encoding platelet-derived growth factor receptor beta. The condition is characterized by the onset of solitary or multicentric benign tumors in the skin, striated muscles, bones, and viscera. The lesions may be present at birth or become apparent in early infancy or even occasionally in adult life." @default.