19926013

Source:http://linkedlifedata.com/resource/pubmed/id/19926013

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0023976, umls-concept:C0332307, umls-concept:C1547011, umls-concept:C1879746
pubmed:issue	22
pubmed:dateCreated	2009-11-20
pubmed:abstractText	The purpose of this study was to investigate the effect of location, coding type, and topology of KCNH2(hERG) mutations on clinical phenotype in type 2 long QT syndrome (LQTS).
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/HL-33843, http://linkedlifedata.com/resource/pubmed/grant/HL-51618, http://linkedlifedata.com/resource/pubmed/grant/HL-60723, http://linkedlifedata.com/resource/pubmed/grant/R01 HL033843-21
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19926013-19926014
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8301365
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, Nonsense, http://linkedlifedata.com/resource/pubmed/chemical/ERG1 potassium channel, http://linkedlifedata.com/resource/pubmed/chemical/Ether-A-Go-Go Potassium Channels
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1558-3597
pubmed:author	pubmed-author:AckermanMichael JMJ, pubmed-author:AminVinitV, pubmed-author:AndrewsMark LML, pubmed-author:GoldenbergIlanI, pubmed-author:HofmanNynkeN, pubmed-author:JanuaryCraig TCT, pubmed-author:KamakuraShiroS, pubmed-author:KaufmanElizabeth SES, pubmed-author:McNittScottS, pubmed-author:MiyamotoYoshihiroY, pubmed-author:MossArthur JAJ, pubmed-author:NodaTakashiT, pubmed-author:QiMingM, pubmed-author:RobinsonJennifer LJL, pubmed-author:ShahSamitS, pubmed-author:ShimizuWataruW, pubmed-author:TesterDavid JDJ, pubmed-author:TowbinJeffrey AJA, pubmed-author:VincentG MichaelGM, pubmed-author:WildeArthur A MAA, pubmed-author:ZarebaWojciechW
pubmed:issnType	Electronic
pubmed:day	24
pubmed:volume	54
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2052-62
pubmed:dateRevised	2011-9-26
pubmed:meshHeading	pubmed-meshheading:19926013-Adolescent, pubmed-meshheading:19926013-Adult, pubmed-meshheading:19926013-Child, pubmed-meshheading:19926013-Codon, Nonsense, pubmed-meshheading:19926013-Ether-A-Go-Go Potassium Channels, pubmed-meshheading:19926013-Female, pubmed-meshheading:19926013-Genotype, pubmed-meshheading:19926013-Humans, pubmed-meshheading:19926013-Long QT Syndrome, pubmed-meshheading:19926013-Male, pubmed-meshheading:19926013-Membrane Potentials, pubmed-meshheading:19926013-Models, Molecular, pubmed-meshheading:19926013-Mutation, Missense, pubmed-meshheading:19926013-Phenotype, pubmed-meshheading:19926013-Proportional Hazards Models, pubmed-meshheading:19926013-Protein Structure, Secondary, pubmed-meshheading:19926013-Retrospective Studies, pubmed-meshheading:19926013-Young Adult
pubmed:year	2009
pubmed:articleTitle	Genotype-phenotype aspects of type 2 long QT syndrome.
pubmed:affiliation	Division of Cardiology, Department of Internal Medicine, National Cardiovascular Center, Suita, Osaka, Japan. wshimizu@hsp.ncvc.go.jp
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural