Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3b6bac448bb4193b0b892dc158a54bca> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B3b6bac448bb4193b0b892dc158a54bca NCIT_P378 "NCI" @default.
- B3b6bac448bb4193b0b892dc158a54bca type Axiom @default.
- B3b6bac448bb4193b0b892dc158a54bca annotatedProperty IAO_0000115 @default.
- B3b6bac448bb4193b0b892dc158a54bca annotatedSource NCIT_C132195 @default.
- B3b6bac448bb4193b0b892dc158a54bca annotatedTarget "An autosomal recessive neurodegenerative condition caused by mutation(s) in the WDR73 gene, encoding WD repeat-containing protein 73. It is characterized by microcephaly and severely delayed psychomotor development." @default.