Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_assertion description "[Considering that approximately 2% of Caucasian controls host rare, nonsynonymous variants in the SCN5A-encoded cardiac sodium channel, caution must be exercised when interpreting SCN5A genetic test results for long QT syndrome (LQTS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_assertion evidence source_evidence_literature NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_assertion SIO_000772 20403459 NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_assertion wasDerivedFrom befree-2016 NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_assertion wasGeneratedBy ECO_0000203 NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.
- befree-2016 importedOn "2016-02-19" NP806929.RAUnRsDy_Og_NfRInxLjQxwoFDft62XT-OLHS0rzdr0no130_provenance.