Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf62b94a6cc1d05ba2ade096ca6397987> ?p ?o ?g. }
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- Bf62b94a6cc1d05ba2ade096ca6397987 hasDbXref "Orphanet:3268" @default.
- Bf62b94a6cc1d05ba2ade096ca6397987 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- Bf62b94a6cc1d05ba2ade096ca6397987 type Axiom @default.
- Bf62b94a6cc1d05ba2ade096ca6397987 annotatedProperty IAO_0000115 @default.
- Bf62b94a6cc1d05ba2ade096ca6397987 annotatedSource MONDO_0011320 @default.
- Bf62b94a6cc1d05ba2ade096ca6397987 annotatedTarget "An extremely rare syndrome characterized by the association of radioulnar synostosis with microcephaly, scoliosis, short stature and intellectual deficit." @default.