Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1b6dc7952deeaddb522c41fb9794887c> ?p ?o ?g. }
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- B1b6dc7952deeaddb522c41fb9794887c hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B1b6dc7952deeaddb522c41fb9794887c type Axiom @default.
- B1b6dc7952deeaddb522c41fb9794887c annotatedProperty IAO_0000115 @default.
- B1b6dc7952deeaddb522c41fb9794887c annotatedSource MONDO_0014929 @default.
- B1b6dc7952deeaddb522c41fb9794887c annotatedTarget "Any retinitis pigmentosa in which the cause of the disease is a mutation in the POMGNT1 gene." @default.