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- Bf66cc28725b7e15ae9c120eafa499419 NCIT_P378 "NCI" @default.
- Bf66cc28725b7e15ae9c120eafa499419 type Axiom @default.
- Bf66cc28725b7e15ae9c120eafa499419 annotatedProperty IAO_0000115 @default.
- Bf66cc28725b7e15ae9c120eafa499419 annotatedSource NCIT_C126810 @default.
- Bf66cc28725b7e15ae9c120eafa499419 annotatedTarget "An autosomal dominant condition presenting with hyponatremia and hyperkalemia, mimicking low concentrations of aldosterone, associated with loss-of-function mutation(s) in the NR3C2 gene, encoding the mineralocorticoid receptor." @default.