20456702

Source:http://linkedlifedata.com/resource/pubmed/id/20456702

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Subject	Predicate	Object	Context
pubmed-article:20456702	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:20456702	lifeskim:mentions	umls-concept:C1412099	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C1762617	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0031437	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0332281	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C1442161	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0002085	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0206243	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0078140	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0679622	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C1706204	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C0205314	lld:lifeskim
pubmed-article:20456702	lifeskim:mentions	umls-concept:C1555721	lld:lifeskim
pubmed-article:20456702	pubmed:issue	7	lld:pubmed
pubmed-article:20456702	pubmed:dateCreated	2010-7-19	lld:pubmed
pubmed-article:20456702	pubmed:abstractText	The 1061delC single-nucleotide polymorphism (SNP) has been reported mostly in the context of the common A(2)[A201] allele and typically produces an A(2) phenotype. This study evaluated new A(weak) alleles, each containing 1061delC.	lld:pubmed
pubmed-article:20456702	pubmed:language	eng	lld:pubmed
pubmed-article:20456702	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:20456702	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:20456702	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:20456702	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:20456702	pubmed:month	Jul	lld:pubmed
pubmed-article:20456702	pubmed:issn	1537-2995	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:HustinxHeinH	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:OlssonMartin...	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:PalcicMonica...	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:JørgensenRené...	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:HellbergAsaA	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:YazerMark HMH	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:PeyrardThierr...	lld:pubmed
pubmed-article:20456702	pubmed:author	pubmed-author:HultAnnika...	lld:pubmed
pubmed-article:20456702	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:20456702	pubmed:volume	50	lld:pubmed
pubmed-article:20456702	pubmed:owner	NLM	lld:pubmed
pubmed-article:20456702	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:20456702	pubmed:pagination	1471-86	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:meshHeading	pubmed-meshheading:20456702...	lld:pubmed
pubmed-article:20456702	pubmed:year	2010	lld:pubmed
pubmed-article:20456702	pubmed:articleTitle	Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.	lld:pubmed
pubmed-article:20456702	pubmed:affiliation	Division of Hematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.	lld:pubmed
pubmed-article:20456702	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:20456702	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
entrez-gene:28	entrezgene:pubmed	pubmed-article:20456702	lld:entrezgene