Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B56c7698a48bdff178823f89e37d2bf1e> ?p ?o ?g. }
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- B56c7698a48bdff178823f89e37d2bf1e hasDbXref "MONDO:design_pattern" @default.
- B56c7698a48bdff178823f89e37d2bf1e type Axiom @default.
- B56c7698a48bdff178823f89e37d2bf1e annotatedProperty hasNarrowSynonym @default.
- B56c7698a48bdff178823f89e37d2bf1e annotatedSource MONDO_0013963 @default.
- B56c7698a48bdff178823f89e37d2bf1e annotatedTarget "autosomal recessive nonsyndromic deafness caused by mutation in CABP2" @default.