Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_assertion description "[ferroportin mutations A77D, V162delta, and G490D are associated with a typical pattern of hemochromatosis disease in vivo ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_assertion evidence source_evidence_literature NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_assertion SIO_000772 15692071 NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_assertion wasDerivedFrom lhgdn-20090331 NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_assertion wasGeneratedBy ECO_0000203 NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148073.RArri4U2QCQ8YhqcsxQ7abZSAVWoa8g7LhThr4c9OWhAE130_provenance.