Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf4bc2f995c8ec647d06e8388b535514a> ?p ?o ?g. }
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- Bf4bc2f995c8ec647d06e8388b535514a hasDbXref "Orphanet:199318" @default.
- Bf4bc2f995c8ec647d06e8388b535514a type Axiom @default.
- Bf4bc2f995c8ec647d06e8388b535514a annotatedProperty IAO_0000115 @default.
- Bf4bc2f995c8ec647d06e8388b535514a annotatedSource MONDO_0012774 @default.
- Bf4bc2f995c8ec647d06e8388b535514a annotatedTarget "15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features." @default.