Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion> ?p ?o ?g. }
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- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion type Assertion NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_head.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_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." NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion evidence source_evidence_literature NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion SIO_000772 21831960 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion wasDerivedFrom befree-2016 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.
- NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_assertion wasGeneratedBy ECO_0000203 NP916131.RAysTDjW9d_DnadaD3ymu9l8ayVgeN6GCeOAK1kKv2x1g130_provenance.