Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion description "[Germline mutations of RET cause a dominantly inherited dysgenesis of the enteric nervous system known as Hirschsprung's disease (HSCR; aganglionosis megacolon).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion evidence source_evidence_literature NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion SIO_000772 10484767 NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion wasDerivedFrom befree-20150227 NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion wasGeneratedBy ECO_0000203 NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_provenance.