Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_assertion description "[The ecNOS gene a/b polymorphism and the NADH/NADPH oxidase p22 phox gene C242T polymorphism were found to be significantly associated with the development of CAD in Korean male patients less than 51 years old.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_assertion evidence source_evidence_literature NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_assertion SIO_000772 11530961 NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_assertion wasDerivedFrom befree-20150227 NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_assertion wasGeneratedBy ECO_0000203 NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP352202.RAFnCmV0d84ZfMxknGb245wb02Umh_Xyd4iubR2CcGE0k130_provenance.