17157483

Source:http://linkedlifedata.com/resource/pubmed/id/17157483

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018591, umls-concept:C0020474, umls-concept:C0030705, umls-concept:C0936012, umls-concept:C1424878
pubmed:issue	1
pubmed:dateCreated	2006-12-26
pubmed:abstractText	Familial combined hyperlipidemia (FCH) is the most common genetic lipid disorder with an undefined genetic etiology. Apolipoprotein A5 gene (APOA5) variants were previously shown to contribute to FCH. The aim of the present study was to evaluate the association of APOA5 variants with FCH and its related phenotypes in Dutch FCH patients. Furthermore, the effects of variants in the APOA5 gene on carotid intima-media thickness (IMT) and cardiovascular disease (CVD) were examined.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0217513
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/APOA5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins A, http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, HDL, http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins, LDL, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0006-3002
pubmed:author	pubmed-author:Dallinga-ThieGeesje MGM, pubmed-author:IsaacsAaronA, pubmed-author:StalenhoefAnton F HAF, pubmed-author:TalmudPhilippa JPJ, pubmed-author:ZengWu-WeiWW, pubmed-author:de GraafJacquelineJ, pubmed-author:ter AvestEwoudE, pubmed-author:van DuijnCornelia MCM, pubmed-author:van der VleutenGerly MGM
pubmed:issnType	Print
pubmed:volume	1772
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	81-8
pubmed:meshHeading	pubmed-meshheading:17157483-Adult, pubmed-meshheading:17157483-Apolipoproteins A, pubmed-meshheading:17157483-Cardiovascular Diseases, pubmed-meshheading:17157483-Carotid Arteries, pubmed-meshheading:17157483-Cholesterol, HDL, pubmed-meshheading:17157483-Female, pubmed-meshheading:17157483-Genetic Predisposition to Disease, pubmed-meshheading:17157483-Haplotypes, pubmed-meshheading:17157483-Homozygote, pubmed-meshheading:17157483-Humans, pubmed-meshheading:17157483-Hyperlipidemia, Familial Combined, pubmed-meshheading:17157483-Lipoproteins, LDL, pubmed-meshheading:17157483-Male, pubmed-meshheading:17157483-Middle Aged, pubmed-meshheading:17157483-Netherlands, pubmed-meshheading:17157483-Polymorphism, Genetic, pubmed-meshheading:17157483-Risk Assessment, pubmed-meshheading:17157483-Triglycerides
pubmed:year	2007
pubmed:articleTitle	Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia.
pubmed:affiliation	Department of Medicine, Division of General Internal Medicine, 463, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't