11112899

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

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002994, umls-concept:C0015295, umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0332183, umls-concept:C1442161, umls-concept:C1515568
pubmed:issue	6
pubmed:dateCreated	2001-1-8
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.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/1275002
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Complement C1 Inactivator Proteins
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0091-6749
pubmed:author	pubmed-author:AgostoniAA, pubmed-author:CarugatiAA, pubmed-author:ChoquetSS, pubmed-author:CicardiMM, pubmed-author:DuponchelCC, pubmed-author:PappalardoEE, pubmed-author:TossGG
pubmed:issnType	Print
pubmed:volume	106
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1147-54
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:11112899-Angioedema, pubmed-meshheading:11112899-Base Sequence, pubmed-meshheading:11112899-Complement C1 Inactivator Proteins, pubmed-meshheading:11112899-Exons, pubmed-meshheading:11112899-Gene Deletion, pubmed-meshheading:11112899-Humans, pubmed-meshheading:11112899-Point Mutation
pubmed:year	2000
pubmed:articleTitle	Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema.
pubmed:affiliation	Unité d'Immunogénétique, Institut National de la Santé et de la Recherche Médicale (INSERM U276), Institut Pasteur, Paris, France.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't