Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- befree-2016 importedOn "2016-02-19" NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_assertion wasGeneratedBy ECO_0000203 NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_assertion wasDerivedFrom befree-2016 NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_assertion SIO_000772 22304542 NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_assertion evidence source_evidence_literature NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.
- NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_assertion description "[The eNOS 894T allele carriers are at greater risk for both MtS and ED, suggesting that eNOS G894T gene polymorphism might play an implication as a common genetic susceptibility factor to develop both disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958458.RA9IbEzzy35h6RCMj3jGkemE-tIEtph3fgSQlx6PgnosY130_provenance.