19525021

Source:http://linkedlifedata.com/resource/pubmed/id/19525021

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018818, umls-concept:C0042333, umls-concept:C1414681
pubmed:issue	1
pubmed:dateCreated	2010-11-5
pubmed:abstractText	To investigate the possible genetic role of FOXH1 in the pathogenesis of ventricular septal defect (VSD).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8200291
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FOXH1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Forkhead Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1874-1754
pubmed:author	pubmed-author:HSUJ YJY, pubmed-author:UdaHH, pubmed-author:WangBinbinB, pubmed-author:WangJingJ, pubmed-author:XieXiaodongX, pubmed-author:YanJintingJ, pubmed-author:ZhouShiyiS
pubmed:copyrightInfo	Copyright © 2009 Elsevier Ireland Ltd. All rights reserved.
pubmed:issnType	Electronic
pubmed:day	5
pubmed:volume	145
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	83-5
pubmed:meshHeading	pubmed-meshheading:19525021-Amino Acid Sequence, pubmed-meshheading:19525021-Asian Continental Ancestry Group, pubmed-meshheading:19525021-Cohort Studies, pubmed-meshheading:19525021-Forkhead Transcription Factors, pubmed-meshheading:19525021-Genetic Variation, pubmed-meshheading:19525021-Heart Septal Defects, Ventricular, pubmed-meshheading:19525021-Humans, pubmed-meshheading:19525021-Molecular Sequence Data, pubmed-meshheading:19525021-Mutation
pubmed:year	2010
pubmed:articleTitle	Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.
pubmed:publicationType	Letter, Comparative Study, Research Support, Non-U.S. Gov't