Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5e149a5705b33806248af027e1f7a27e> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5e149a5705b33806248af027e1f7a27e hasDbXref "NCIT:C84543-modified" @default.
- B5e149a5705b33806248af027e1f7a27e type Axiom @default.
- B5e149a5705b33806248af027e1f7a27e annotatedProperty IAO_0000115 @default.
- B5e149a5705b33806248af027e1f7a27e annotatedSource MONDO_0043209 @default.
- B5e149a5705b33806248af027e1f7a27e annotatedTarget "A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair, or skin." @default.