Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4be754953a6d2c87405fc6746e0d2b9c> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B4be754953a6d2c87405fc6746e0d2b9c NCIT_P378 "NCI" @default.
- B4be754953a6d2c87405fc6746e0d2b9c type Axiom @default.
- B4be754953a6d2c87405fc6746e0d2b9c annotatedProperty IAO_0000115 @default.
- B4be754953a6d2c87405fc6746e0d2b9c annotatedSource NCIT_C75015 @default.
- B4be754953a6d2c87405fc6746e0d2b9c annotatedTarget "A rare autosomal dominant syndrome linked to mutations in the PITX2 gene. It is characterized by abnormalities in the anterior chamber of the eye and underdevelopment of the teeth." @default.