Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8ba7f4b4f1dd08dfd19278458672de8e> ?p ?o ?g. }
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- B8ba7f4b4f1dd08dfd19278458672de8e NCIT_P378 "NCI" @default.
- B8ba7f4b4f1dd08dfd19278458672de8e type Axiom @default.
- B8ba7f4b4f1dd08dfd19278458672de8e annotatedProperty IAO_0000115 @default.
- B8ba7f4b4f1dd08dfd19278458672de8e annotatedSource NCIT_C75008 @default.
- B8ba7f4b4f1dd08dfd19278458672de8e annotatedTarget "A rare autosomal dominant syndrome caused by mutations in the PAX3 gene. It is characterized by hearing loss, dystopia canthorum (widely spaced inner corners of the eyes), and changes in the color of the skin, hair, and eyes." @default.