Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_assertion description "[In addition, an E229K CYP1B1 mutation was found in a woman with a germ line HNF1alpha mutation in a familial adenomatosis context.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_assertion evidence source_evidence_literature NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_assertion SIO_000772 17363580 NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_assertion wasDerivedFrom befree-20140225 NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_assertion wasGeneratedBy ECO_0000203 NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP403761.RA1YTqND6EG2NG9OWV16gkbJ5o7d7Onz2DdpjLaaz2rOY130_provenance.