Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_assertion description "[The rare linked Cx40 polymorphisms are associated with enhanced CD and thus with the substrate for reentry in AF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_assertion evidence source_evidence_literature NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_assertion SIO_000772 16646598 NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_assertion wasDerivedFrom gad-20130706 NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_assertion wasGeneratedBy ECO_0000203 NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP43582.RA0QiFmL0BGKVKAwA7ILVI6ZbcJTSLs3kmYfuonw7jtgw130_provenance.