Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_assertion wasGeneratedBy ECO_0000203 NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_assertion wasDerivedFrom befree-20140225 NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_assertion SIO_000772 19822806 NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_assertion evidence source_evidence_literature NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_assertion description "[NOS1AP variants were significantly associated with the occurrence of symptoms (rs4657139, P=0.019; rs16847548, P=0.003), with clinical severity, as manifested by a greater probability for cardiac arrest and sudden death (rs4657139, P=0.028; rs16847548, P=0.014), and with greater likelihood of having a QT interval in the top 40% of values among all mutation carriers (rs4657139, P=0.03; rs16847548, P=0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP600920.RAB6ES1Bt-DaKWunjJfs1SYqOGFb5QLWuBbAy0Rl1Cx7I130_provenance.