Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3fa14b826bff07e96e4c5bffa7e77114> ?p ?o ?g. }
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- B3fa14b826bff07e96e4c5bffa7e77114 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B3fa14b826bff07e96e4c5bffa7e77114 hasDbXref "MONDO:patterns/inherited_susceptibility" @default.
- B3fa14b826bff07e96e4c5bffa7e77114 type Axiom @default.
- B3fa14b826bff07e96e4c5bffa7e77114 annotatedProperty IAO_0000115 @default.
- B3fa14b826bff07e96e4c5bffa7e77114 annotatedSource MONDO_0012763 @default.
- B3fa14b826bff07e96e4c5bffa7e77114 annotatedTarget "An inherited susceptibility or predisposition to developing child absence epilepsy or idiopathic generalized epilepsy, in which the cause of the disease is a mutation in the CACNA1H gene." @default.