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- NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_assertion type Assertion NP671034.RA0wBu79RfRPSWkQrCFSEiaoQnSXd6fQYZDw632vExUxg130_head.
- 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.