Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:20888888rdf:typepubmed:Citationlld:pubmed
pubmed-article:20888888lifeskim:mentionsumls-concept:C0030705lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0023467lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0017337lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0205341lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1511473lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0332281lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0040624lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1514562lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1883221lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1882417lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C2587213lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0439661lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C0936012lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1883204lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1880389lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C1707513lld:lifeskim
pubmed-article:20888888lifeskim:mentionsumls-concept:C2362652lld:lifeskim
pubmed-article:20888888pubmed:issue1lld:pubmed
pubmed-article:20888888pubmed:dateCreated2010-12-20lld:pubmed
pubmed-article:20888888pubmed:abstractTextCEBPA-mutated normal karyotype acute myeloid leukemia (AML) has recently been included as a provisional entity in the World Health Organization classification. The CEBPA mutations are heterogeneous, including missense/nonsense base exchanges, frameshift mutations, and insertions/deletions being distributed throughout the gene. One of the genetic alterations within CEBPA (c.1175_1180dup; p.P194_H195dup) was later suggested to represent an inherited polymorphism. As this is not a simple single nucleotide polymorphism, but a six-base pair insertion that leads to a two amino acid elongation of the protein, functional implications cannot be excluded.lld:pubmed
pubmed-article:20888888pubmed:languageenglld:pubmed
pubmed-article:20888888pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:20888888pubmed:citationSubsetIMlld:pubmed
pubmed-article:20888888pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:20888888pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:20888888pubmed:statusMEDLINElld:pubmed
pubmed-article:20888888pubmed:monthJanlld:pubmed
pubmed-article:20888888pubmed:issn1873-2399lld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:LohsePeterPlld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:SchnittgerSus...lld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:HaferlachTors...lld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:KernWolfgangWlld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:BacherUlrikeUlld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:HaferlachClau...lld:pubmed
pubmed-article:20888888pubmed:authorpubmed-author:EderChristian...lld:pubmed
pubmed-article:20888888pubmed:copyrightInfoCopyright © 2011 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.lld:pubmed
pubmed-article:20888888pubmed:issnTypeElectroniclld:pubmed
pubmed-article:20888888pubmed:volume39lld:pubmed
pubmed-article:20888888pubmed:ownerNLMlld:pubmed
pubmed-article:20888888pubmed:authorsCompleteYlld:pubmed
pubmed-article:20888888pubmed:pagination87-94lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:meshHeadingpubmed-meshheading:20888888...lld:pubmed
pubmed-article:20888888pubmed:year2011lld:pubmed
pubmed-article:20888888pubmed:articleTitleA copy number repeat polymorphism in the transactivation domain of the CEPBA gene is possibly associated with a protective effect against acquired CEBPA mutations: an analysis in 1135 patients with AML and 187 healthy controls.lld:pubmed
pubmed-article:20888888pubmed:affiliationMLL Munich Leukemia Laboratory, Munich, Germany. Susanne.Schnittger@mll-online.comlld:pubmed
pubmed-article:20888888pubmed:publicationTypeJournal Articlelld:pubmed
entrez-gene:1050entrezgene:pubmedpubmed-article:20888888lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:20888888lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:20888888lld:entrezgene