Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3e8c79d8884ffaf736ff5f33b2acd553> ?p ?o ?g. }
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- B3e8c79d8884ffaf736ff5f33b2acd553 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B3e8c79d8884ffaf736ff5f33b2acd553 type Axiom @default.
- B3e8c79d8884ffaf736ff5f33b2acd553 annotatedProperty IAO_0000115 @default.
- B3e8c79d8884ffaf736ff5f33b2acd553 annotatedSource MONDO_0012562 @default.
- B3e8c79d8884ffaf736ff5f33b2acd553 annotatedTarget "Any holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene." @default.