Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:2792129rdf:typepubmed:Citationlld:pubmed
pubmed-article:2792129lifeskim:mentionsumls-concept:C0025303lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0241888lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0009498lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C1179435lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0034897lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0332281lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0011155lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C1705248lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C1548799lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C1524073lld:lifeskim
pubmed-article:2792129lifeskim:mentionsumls-concept:C0449432lld:lifeskim
pubmed-article:2792129pubmed:issue8lld:pubmed
pubmed-article:2792129pubmed:dateCreated1989-11-2lld:pubmed
pubmed-article:2792129pubmed:abstractTextWe describe an 11-year-old girl suffering from recurrent meningitis with a complete absence of the seventh component of complement (C7). Diagnosis was established by haemolytic titration and western blotting. The patient's serum lacked the 85 kDa C7 chain. Haemolytic activity of serum was reconstituted with either pooled normal human serum or with purified C7. The relatives (parents and one sister) had half-normal levels of both immunochemically and functionally determined C7, indicating a heterozygous state for C7 deficiency.lld:pubmed
pubmed-article:2792129pubmed:languageenglld:pubmed
pubmed-article:2792129pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2792129pubmed:citationSubsetIMlld:pubmed
pubmed-article:2792129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:2792129pubmed:statusMEDLINElld:pubmed
pubmed-article:2792129pubmed:monthAuglld:pubmed
pubmed-article:2792129pubmed:issn0340-6199lld:pubmed
pubmed-article:2792129pubmed:authorpubmed-author:SegerRRlld:pubmed
pubmed-article:2792129pubmed:authorpubmed-author:WahlHHlld:pubmed
pubmed-article:2792129pubmed:authorpubmed-author:PietschHHlld:pubmed
pubmed-article:2792129pubmed:authorpubmed-author:NürnbergerWWlld:pubmed
pubmed-article:2792129pubmed:authorpubmed-author:BufonTTlld:pubmed
pubmed-article:2792129pubmed:issnTypePrintlld:pubmed
pubmed-article:2792129pubmed:volume148lld:pubmed
pubmed-article:2792129pubmed:ownerNLMlld:pubmed
pubmed-article:2792129pubmed:authorsCompleteYlld:pubmed
pubmed-article:2792129pubmed:pagination758-60lld:pubmed
pubmed-article:2792129pubmed:dateRevised2005-11-17lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:meshHeadingpubmed-meshheading:2792129-...lld:pubmed
pubmed-article:2792129pubmed:year1989lld:pubmed
pubmed-article:2792129pubmed:articleTitleFamilial deficiency of the seventh component of complement associated with recurrent meningococcal infections.lld:pubmed
pubmed-article:2792129pubmed:affiliationAbteilung für Neonatologie und Gastroenterologie der Universität, Düsseldorf, Federal Republic of Germany.lld:pubmed
pubmed-article:2792129pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2792129pubmed:publicationTypeCase Reportslld:pubmed
entrez-gene:730entrezgene:pubmedpubmed-article:2792129lld:entrezgene
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:2792129lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:2792129lld:pubmed