Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B89b9fe5341fb8b0a6976ea92b61d4fb5> ?p ?o ?g. }
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- B89b9fe5341fb8b0a6976ea92b61d4fb5 hasDbXref "MONDO:design_pattern" @default.
- B89b9fe5341fb8b0a6976ea92b61d4fb5 type Axiom @default.
- B89b9fe5341fb8b0a6976ea92b61d4fb5 annotatedProperty hasExactSynonym @default.
- B89b9fe5341fb8b0a6976ea92b61d4fb5 annotatedSource MONDO_0012695 @default.
- B89b9fe5341fb8b0a6976ea92b61d4fb5 annotatedTarget "Meckel syndrome caused by mutation in RPGRIP1L" @default.