Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1d0b9e4f71f747fac205369f87fc3158> ?p ?o ?g. }
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- B1d0b9e4f71f747fac205369f87fc3158 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B1d0b9e4f71f747fac205369f87fc3158 type Axiom @default.
- B1d0b9e4f71f747fac205369f87fc3158 annotatedProperty IAO_0000115 @default.
- B1d0b9e4f71f747fac205369f87fc3158 annotatedSource MONDO_0013805 @default.
- B1d0b9e4f71f747fac205369f87fc3158 annotatedTarget "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the DYNC1H1 gene." @default.