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- Be9b1a8242ad8c1ebbe42231356774fcd hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Be9b1a8242ad8c1ebbe42231356774fcd hasDbXref "MONDO:patterns/inherited_susceptibility" @default.
- Be9b1a8242ad8c1ebbe42231356774fcd type Axiom @default.
- Be9b1a8242ad8c1ebbe42231356774fcd annotatedProperty IAO_0000115 @default.
- Be9b1a8242ad8c1ebbe42231356774fcd annotatedSource MONDO_0012763 @default.
- Be9b1a8242ad8c1ebbe42231356774fcd 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.