Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B78386b9f84d6b75abdc52e3831bef29b> ?p ?o ?g. }
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- B78386b9f84d6b75abdc52e3831bef29b hasDbXref "MONDO:design_pattern" @default.
- B78386b9f84d6b75abdc52e3831bef29b type Axiom @default.
- B78386b9f84d6b75abdc52e3831bef29b annotatedProperty hasExactSynonym @default.
- B78386b9f84d6b75abdc52e3831bef29b annotatedSource MONDO_0013266 @default.
- B78386b9f84d6b75abdc52e3831bef29b annotatedTarget "autosomal dominant non-syndromic intellectual disability caused by mutation in MEF2C" @default.