11593646

Source:http://linkedlifedata.com/resource/pubmed/id/11593646

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Subject	Predicate	Object	Context
pubmed-article:11593646	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:11593646	lifeskim:mentions	umls-concept:C0020792	lld:lifeskim
pubmed-article:11593646	lifeskim:mentions	umls-concept:C0332307	lld:lifeskim
pubmed-article:11593646	lifeskim:mentions	umls-concept:C0015306	lld:lifeskim
pubmed-article:11593646	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:11593646	lifeskim:mentions	umls-concept:C1332838	lld:lifeskim
pubmed-article:11593646	pubmed:issue	1	lld:pubmed
pubmed-article:11593646	pubmed:dateCreated	2001-10-11	lld:pubmed
pubmed-article:11593646	pubmed:abstractText	To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type II (EXT2) in affected members of EXT families so as to confirm that it is the disease-causing gene.	lld:pubmed
pubmed-article:11593646	pubmed:language	eng	lld:pubmed
pubmed-article:11593646	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11593646	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:11593646	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11593646	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11593646	pubmed:month	Jan	lld:pubmed
pubmed-article:11593646	pubmed:issn	0366-6999	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:WangDD	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:YUMM	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:LiHH	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:ZhouJJ	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:PanQQ	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:LongZZ	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:DengHH	lld:pubmed
pubmed-article:11593646	pubmed:author	pubmed-author:XiaJJ	lld:pubmed
pubmed-article:11593646	pubmed:issnType	Print	lld:pubmed
pubmed-article:11593646	pubmed:volume	112	lld:pubmed
pubmed-article:11593646	pubmed:owner	NLM	lld:pubmed
pubmed-article:11593646	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11593646	pubmed:pagination	72-5	lld:pubmed
pubmed-article:11593646	pubmed:dateRevised	2006-11-15	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:meshHeading	pubmed-meshheading:11593646...	lld:pubmed
pubmed-article:11593646	pubmed:year	1999	lld:pubmed
pubmed-article:11593646	pubmed:articleTitle	Identification of mutation in a candidate gene for hereditary multiple exostoses type II.	lld:pubmed
pubmed-article:11593646	pubmed:affiliation	National Laboratory of Medical Genetics, Hunan Medical University, Changsha 410078, China.	lld:pubmed
pubmed-article:11593646	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:11593646	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
http://linkedlifedata.com/r...	pubmed:referesTo	pubmed-article:11593646	lld:pubmed