Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1d4792d7e324468e6dbc894743e29f56> ?p ?o ?g. }
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- B1d4792d7e324468e6dbc894743e29f56 hasDbXref "MONDO:design_pattern" @default.
- B1d4792d7e324468e6dbc894743e29f56 type Axiom @default.
- B1d4792d7e324468e6dbc894743e29f56 annotatedProperty hasExactSynonym @default.
- B1d4792d7e324468e6dbc894743e29f56 annotatedSource MONDO_0014002 @default.
- B1d4792d7e324468e6dbc894743e29f56 annotatedTarget "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1" @default.