11112899

Source:http://linkedlifedata.com/resource/pubmed/id/11112899

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Subject	Predicate	Object	Context
pubmed-article:11112899	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0030705	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0002994	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0017337	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0026882	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C1442161	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0015295	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C1515568	lld:lifeskim
pubmed-article:11112899	lifeskim:mentions	umls-concept:C0332183	lld:lifeskim
pubmed-article:11112899	pubmed:issue	6	lld:pubmed
pubmed-article:11112899	pubmed:dateCreated	2001-1-8	lld:pubmed
pubmed-article:11112899	pubmed:abstractText	Cases of angioedema with no family history but with functionally low levels of C1 inhibitor and recurrent attacks are often observed. Clinical and biochemical data do not distinguish these cases from proven inherited forms of hereditary angioedema.	lld:pubmed
pubmed-article:11112899	pubmed:language	eng	lld:pubmed
pubmed-article:11112899	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11112899	pubmed:citationSubset	AIM	lld:pubmed
pubmed-article:11112899	pubmed:chemical	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:11112899	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11112899	pubmed:month	Dec	lld:pubmed
pubmed-article:11112899	pubmed:issn	0091-6749	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:TossGG	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:AgostoniAA	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:CicardiMM	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:DuponchelCC	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:CarugatiAA	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:PappalardoEE	lld:pubmed
pubmed-article:11112899	pubmed:author	pubmed-author:ChoquetSS	lld:pubmed
pubmed-article:11112899	pubmed:issnType	Print	lld:pubmed
pubmed-article:11112899	pubmed:volume	106	lld:pubmed
pubmed-article:11112899	pubmed:owner	NLM	lld:pubmed
pubmed-article:11112899	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11112899	pubmed:pagination	1147-54	lld:pubmed
pubmed-article:11112899	pubmed:dateRevised	2007-11-15	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:meshHeading	pubmed-meshheading:11112899...	lld:pubmed
pubmed-article:11112899	pubmed:year	2000	lld:pubmed
pubmed-article:11112899	pubmed:articleTitle	Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema.	lld:pubmed
pubmed-article:11112899	pubmed:affiliation	Unité d'Immunogénétique, Institut National de la Santé et de la Recherche Médicale (INSERM U276), Institut Pasteur, Paris, France.	lld:pubmed
pubmed-article:11112899	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:11112899	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
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http://linkedlifedata.com/r...	pubmed:referesTo	pubmed-article:11112899	lld:pubmed
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