Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B01c20f26640ad5c34b724b4e4736b589> ?p ?o ?g. }
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- B01c20f26640ad5c34b724b4e4736b589 hasDbXref "NCIT:C129030" @default.
- B01c20f26640ad5c34b724b4e4736b589 type Axiom @default.
- B01c20f26640ad5c34b724b4e4736b589 annotatedProperty IAO_0000115 @default.
- B01c20f26640ad5c34b724b4e4736b589 annotatedSource MONDO_0013700 @default.
- B01c20f26640ad5c34b724b4e4736b589 annotatedTarget "An autosomal recessive disorder caused by mutation(s) in the PNLIP gene, encoding pancreatic triacylglycerol lipase. The condition is characterized by absent or reduced pancreatic lipase." @default.