Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_assertion description "[Subgroup analysis showed that the presence of the K897T polymorphism in the LQT2 gene in an affected family was associated with an 11-fold (P=0.001) increase in the risk of recurrent syncope in genotype-negative subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_assertion evidence source_evidence_literature NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_assertion SIO_000772 21831960 NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_assertion wasDerivedFrom befree-20150227 NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_assertion wasGeneratedBy ECO_0000203 NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521911.RAHHgGZ2i-aQip9IfXgZLP3TYQpBSW_lQEzbZ9OTTSAPk130_provenance.