Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion> ?p ?o ?g. }
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- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion type Assertion NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_head.
- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_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." NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_provenance.
- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion evidence source_evidence_literature NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_provenance.
- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion SIO_000772 18436145 NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_provenance.
- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion wasDerivedFrom befree-2016 NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_provenance.
- NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_assertion wasGeneratedBy ECO_0000203 NP667761.RAYctdgDAes88J5US6E7hHvpIl0ebDI0jZy3rlYWKq4WE130_provenance.