Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B61e66ede812fd5a1d4210fb6de064def> ?p ?o ?g. }
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- B61e66ede812fd5a1d4210fb6de064def NCIT_P378 "NCI" @default.
- B61e66ede812fd5a1d4210fb6de064def type Axiom @default.
- B61e66ede812fd5a1d4210fb6de064def annotatedProperty IAO_0000115 @default.
- B61e66ede812fd5a1d4210fb6de064def annotatedSource NCIT_C126810 @default.
- B61e66ede812fd5a1d4210fb6de064def 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.