pubmed-article:17576865 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C1560305 | lld:lifeskim |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C1826455 | lld:lifeskim |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:17576865 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
pubmed-article:17576865 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:17576865 | pubmed:dateCreated | 2007-7-3 | lld:pubmed |
pubmed-article:17576865 | pubmed:abstractText | QT prolongation is an important risk factor for sudden cardiac death. About 35% of QT-interval variation is heritable. In a recent genome-wide association study, a common variant (rs10494366) in the nitric oxide synthase 1 adaptor protein (NOS1AP) gene was found to be associated with QT-interval variation. We tested for association of 2 NOS1AP variants with QT duration and sudden cardiac death. | lld:pubmed |
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pubmed-article:17576865 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17576865 | pubmed:language | eng | lld:pubmed |
pubmed-article:17576865 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17576865 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:17576865 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17576865 | pubmed:month | Jul | lld:pubmed |
pubmed-article:17576865 | pubmed:issn | 1524-4539 | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:HofmanAlbertA | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:WittemanJacqu... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:StrickerBruno... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:UitterlindenA... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:KorsJan AJA | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:de... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:Newton-ChehCh... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:StrausSabine... | lld:pubmed |
pubmed-article:17576865 | pubmed:author | pubmed-author:AarnoudseAlbe... | lld:pubmed |
pubmed-article:17576865 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17576865 | pubmed:day | 3 | lld:pubmed |
pubmed-article:17576865 | pubmed:volume | 116 | lld:pubmed |
pubmed-article:17576865 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17576865 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17576865 | pubmed:pagination | 10-6 | lld:pubmed |
pubmed-article:17576865 | pubmed:dateRevised | 2008-1-9 | lld:pubmed |
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pubmed-article:17576865 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17576865 | pubmed:articleTitle | Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study. | lld:pubmed |
pubmed-article:17576865 | pubmed:affiliation | Department of Epidemiology and Biostatistics, Erasmus Medical Center, PO Box 2040, 3000 CA, Rotterdam, The Netherlands. | lld:pubmed |
pubmed-article:17576865 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17576865 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:17576865 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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