Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_assertion type Assertion NP916129.RA73X7X7gqMSa5S7tGTmV7oIP-0EEZJlNb9Q5o04YKYj0130_head.
- 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.