Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_assertion description "[Cardiac sodium channel dysfunction caused by mutations in the SCN5A gene is associated with a number of relatively uncommon arrhythmia syndromes, including long-QT syndrome type 3 (LQT3), Brugada syndrome, conduction disease, sinus node dysfunction, and atrial standstill, which potentially lead to fatal arrhythmias in relatively young individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_assertion evidence source_evidence_literature NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_assertion SIO_000772 18436145 NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_assertion wasDerivedFrom befree-20150227 NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_assertion wasGeneratedBy ECO_0000203 NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683124.RA3txNlyyFWMmmWqm4rYRQT1q_tzGhWJNYQyBMi6NhpY8130_provenance.