Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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.
- 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." 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.
- NP839116.RAgOZJECkgVbOU2dVDX1z7Jd2xJXK4X4BYNxePvYNSAWo130_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." NP839116.RAgOZJECkgVbOU2dVDX1z7Jd2xJXK4X4BYNxePvYNSAWo130_provenance.