Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc9a39057e0bcc7ecde6d91f6baab3add> ?p ?o ?g. }
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- Bc9a39057e0bcc7ecde6d91f6baab3add hasDbXref "Orphanet:261600" @default.
- Bc9a39057e0bcc7ecde6d91f6baab3add type Axiom @default.
- Bc9a39057e0bcc7ecde6d91f6baab3add annotatedProperty hasExactSynonym @default.
- Bc9a39057e0bcc7ecde6d91f6baab3add annotatedSource MONDO_0016861 @default.
- Bc9a39057e0bcc7ecde6d91f6baab3add annotatedTarget "Alagille-Watson syndrome due to monosomy 20p12" @default.