Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bd8e8a3e32d430fbb842b7c8ed599dc2c> ?p ?o ?g. }
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- Bd8e8a3e32d430fbb842b7c8ed599dc2c hasDbXref "NCIT:C132293" @default.
- Bd8e8a3e32d430fbb842b7c8ed599dc2c type Axiom @default.
- Bd8e8a3e32d430fbb842b7c8ed599dc2c annotatedProperty IAO_0000115 @default.
- Bd8e8a3e32d430fbb842b7c8ed599dc2c annotatedSource MONDO_0010397 @default.
- Bd8e8a3e32d430fbb842b7c8ed599dc2c annotatedTarget "An X-linked recessive condition caused by mutation(s) in the MECP2 gene, encoding methyl-CpG-binding protein 2. It is characterized by severe neonatal encephalopathy." @default.