Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_assertion description "[Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_assertion evidence source_evidence_literature NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_assertion SIO_000772 18752142 NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_assertion wasDerivedFrom gad-20150221 NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_assertion wasGeneratedBy ECO_0000203 NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116302.RAYiDl_ryjsfz34pzFLXhhaPwqVygyFR0U4LhaLjOAR9c130_provenance.