18673462

Source:http://linkedlifedata.com/resource/pubmed/id/18673462

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Subject	Predicate	Object	Context
pubmed-article:18673462	rdf:type	pubmed:Citation	lld:pubmed
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pubmed-article:18673462	lifeskim:mentions	umls-concept:C2700640	lld:lifeskim
pubmed-article:18673462	lifeskim:mentions	umls-concept:C0522498	lld:lifeskim
pubmed-article:18673462	pubmed:issue	3	lld:pubmed
pubmed-article:18673462	pubmed:dateCreated	2009-2-24	lld:pubmed
pubmed-article:18673462	pubmed:language	eng	lld:pubmed
pubmed-article:18673462	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:18673462	pubmed:citationSubset	IM	lld:pubmed
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pubmed-article:18673462	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:18673462	pubmed:month	Mar	lld:pubmed
pubmed-article:18673462	pubmed:issn	1365-2265	lld:pubmed
pubmed-article:18673462	pubmed:author	pubmed-author:EllardSianS	lld:pubmed
pubmed-article:18673462	pubmed:author	pubmed-author:VaidyaBijayB	lld:pubmed
pubmed-article:18673462	pubmed:author	pubmed-author:StalsKarenK	lld:pubmed
pubmed-article:18673462	pubmed:author	pubmed-author:OwensMartinaM	lld:pubmed
pubmed-article:18673462	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:18673462	pubmed:volume	70	lld:pubmed
pubmed-article:18673462	pubmed:owner	NLM	lld:pubmed
pubmed-article:18673462	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:18673462	pubmed:pagination	499-500	lld:pubmed
pubmed-article:18673462	pubmed:dateRevised	2011-11-17	lld:pubmed
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pubmed-article:18673462	pubmed:meshHeading	pubmed-meshheading:18673462...	lld:pubmed
pubmed-article:18673462	pubmed:year	2009	lld:pubmed
pubmed-article:18673462	pubmed:articleTitle	Germline mutations in the CDKN1B gene encoding p27 Kip1 are a rare cause of multiple endocrine neoplasia type 1.	lld:pubmed
pubmed-article:18673462	pubmed:publicationType	Letter	lld:pubmed
entrez-gene:1027	entrezgene:pubmed	pubmed-article:18673462	lld:entrezgene
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