Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1c3379a05c9af0e86f51965c36d4792d> ?p ?o ?g. }
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- B1c3379a05c9af0e86f51965c36d4792d hasDbXref "MONDO:design_pattern" @default.
- B1c3379a05c9af0e86f51965c36d4792d type Axiom @default.
- B1c3379a05c9af0e86f51965c36d4792d annotatedProperty hasExactSynonym @default.
- B1c3379a05c9af0e86f51965c36d4792d annotatedSource MONDO_0013655 @default.
- B1c3379a05c9af0e86f51965c36d4792d annotatedTarget "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1" @default.