12798584

Source:http://linkedlifedata.com/resource/pubmed/id/12798584

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0017347, umls-concept:C0018787, umls-concept:C0018817, umls-concept:C0026882, umls-concept:C0152021, umls-concept:C0152101, umls-concept:C1413784
pubmed:issue	11
pubmed:dateCreated	2003-6-11
pubmed:abstractText	We sought to examine the importance of mutations in the cardiac transcription factor gene NKX2-5 in patients with an atrial septal defect (ASD), patent foramen ovale (PFO), or hypoplastic left heart syndrome (HLHS).
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01 HL 68885-01
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8301365
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/NKX2-5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Xenopus Proteins
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0735-1097
pubmed:author	pubmed-author:ChandarSuchitraS, pubmed-author:ElliottDavid ADA, pubmed-author:FatkinDianeD, pubmed-author:FeneleyMichaelM, pubmed-author:GrossfeldPaulP, pubmed-author:HarveyRichard PRP, pubmed-author:HayesPeterP, pubmed-author:JonesOwenO, pubmed-author:KirkEdwin PEP, pubmed-author:McKenzieFionaF, pubmed-author:TaylorPeterP, pubmed-author:YeohThomasT
pubmed:issnType	Print
pubmed:day	4
pubmed:volume	41
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2072-6
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:12798584-Adolescent, pubmed-meshheading:12798584-Adult, pubmed-meshheading:12798584-Aged, pubmed-meshheading:12798584-Aged, 80 and over, pubmed-meshheading:12798584-Australia, pubmed-meshheading:12798584-Child, pubmed-meshheading:12798584-Child, Preschool, pubmed-meshheading:12798584-Cohort Studies, pubmed-meshheading:12798584-Family Health, pubmed-meshheading:12798584-Female, pubmed-meshheading:12798584-Genes, Homeobox, pubmed-meshheading:12798584-Genetic Markers, pubmed-meshheading:12798584-Heart Block, pubmed-meshheading:12798584-Heart Conduction System, pubmed-meshheading:12798584-Heart Defects, Congenital, pubmed-meshheading:12798584-Heart Septal Defects, Atrial, pubmed-meshheading:12798584-Homeodomain Proteins, pubmed-meshheading:12798584-Humans, pubmed-meshheading:12798584-Hypoplastic Left Heart Syndrome, pubmed-meshheading:12798584-Infant, pubmed-meshheading:12798584-Infant, Newborn, pubmed-meshheading:12798584-Male, pubmed-meshheading:12798584-Middle Aged, pubmed-meshheading:12798584-Point Mutation, pubmed-meshheading:12798584-Polymorphism, Genetic, pubmed-meshheading:12798584-Retrospective Studies, pubmed-meshheading:12798584-Statistics as Topic, pubmed-meshheading:12798584-Transcription Factors, pubmed-meshheading:12798584-United States, pubmed-meshheading:12798584-Xenopus Proteins
pubmed:year	2003
pubmed:articleTitle	Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
pubmed:affiliation	Victor Chang Cardiac Research Institute, 384 Victoria Street, Darlinghurst 2010, Sydney, Australia.
pubmed:publicationType	Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Evaluation Studies