Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1a3db5ade1bc6e6620b45c18bf4794b3> ?p ?o ?g. }
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- B1a3db5ade1bc6e6620b45c18bf4794b3 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B1a3db5ade1bc6e6620b45c18bf4794b3 type Axiom @default.
- B1a3db5ade1bc6e6620b45c18bf4794b3 annotatedProperty IAO_0000115 @default.
- B1a3db5ade1bc6e6620b45c18bf4794b3 annotatedSource MONDO_0013264 @default.
- B1a3db5ade1bc6e6620b45c18bf4794b3 annotatedTarget "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the OPTN gene." @default.