Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B28ad9340eb997c137ab4c8a10f4fe4e3> ?p ?o ?g. }
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- B28ad9340eb997c137ab4c8a10f4fe4e3 hasDbXref "NCIT:C123263" @default.
- B28ad9340eb997c137ab4c8a10f4fe4e3 type Axiom @default.
- B28ad9340eb997c137ab4c8a10f4fe4e3 annotatedProperty IAO_0000115 @default.
- B28ad9340eb997c137ab4c8a10f4fe4e3 annotatedSource MONDO_0018100 @default.
- B28ad9340eb997c137ab4c8a10f4fe4e3 annotatedTarget "A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration." @default.