11069461

Source:http://linkedlifedata.com/resource/pubmed/id/11069461

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Subject	Predicate	Object	Context
pubmed-article:11069461	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:11069461	lifeskim:mentions	umls-concept:C0015576	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C1556085	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C0439660	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C0017337	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C0796348	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C1708726	lld:lifeskim
pubmed-article:11069461	lifeskim:mentions	umls-concept:C2931059	lld:lifeskim
pubmed-article:11069461	pubmed:issue	4	lld:pubmed
pubmed-article:11069461	pubmed:dateCreated	2000-11-20	lld:pubmed
pubmed-article:11069461	pubmed:abstractText	Hypotrichosis of the Marie Unna type (HMU) is a rare autosomal dominant disorder characterized by male-pattern hair loss with childhood onset and anomalies of the hair shaft.	lld:pubmed
pubmed-article:11069461	pubmed:language	eng	lld:pubmed
pubmed-article:11069461	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11069461	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:11069461	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11069461	pubmed:month	Oct	lld:pubmed
pubmed-article:11069461	pubmed:issn	0007-0963	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:ProppingPP	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:KnappMM	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:LVOVAT NTN	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:AltlandKK	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:NöthenM MMM	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:CichonSS	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:AnkerMM	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:KukukGG	lld:pubmed
pubmed-article:11069461	pubmed:author	pubmed-author:HillmerA MAM	lld:pubmed
pubmed-article:11069461	pubmed:issnType	Print	lld:pubmed
pubmed-article:11069461	pubmed:volume	143	lld:pubmed
pubmed-article:11069461	pubmed:owner	NLM	lld:pubmed
pubmed-article:11069461	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11069461	pubmed:pagination	811-4	lld:pubmed
pubmed-article:11069461	pubmed:dateRevised	2006-11-15	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:meshHeading	pubmed-meshheading:11069461...	lld:pubmed
pubmed-article:11069461	pubmed:year	2000	lld:pubmed
pubmed-article:11069461	pubmed:articleTitle	A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.	lld:pubmed
pubmed-article:11069461	pubmed:affiliation	Institute of Human Genetics, University of Bonn, Wilhelmstr. 31, 53111 Bonn, Germany. cichon@mailer.meb.uni-bonn.de	lld:pubmed
pubmed-article:11069461	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:11069461	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed