Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- befree-2016 importedOn "2016-02-19" NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion wasGeneratedBy ECO_0000203 NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion wasDerivedFrom befree-2016 NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion SIO_000772 21831960 NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion evidence source_evidence_literature NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_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." NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_provenance.