Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1ae1f4e9b1b21a2a9f9150c658dcd19e> ?p ?o ?g. }
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- B1ae1f4e9b1b21a2a9f9150c658dcd19e hasDbXref "OMIM:300673" @default.
- B1ae1f4e9b1b21a2a9f9150c658dcd19e type Axiom @default.
- B1ae1f4e9b1b21a2a9f9150c658dcd19e annotatedProperty hasRelatedSynonym @default.
- B1ae1f4e9b1b21a2a9f9150c658dcd19e annotatedSource MONDO_0010397 @default.
- B1ae1f4e9b1b21a2a9f9150c658dcd19e annotatedTarget "encephalopathy, neonatal severe, due to MECP2 mutations" @default.