Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:21868628rdf:typepubmed:Citationlld:pubmed
pubmed-article:21868628lifeskim:mentionsumls-concept:C0042133lld:lifeskim
pubmed-article:21868628lifeskim:mentionsumls-concept:C0017337lld:lifeskim
pubmed-article:21868628lifeskim:mentionsumls-concept:C0026882lld:lifeskim
pubmed-article:21868628lifeskim:mentionsumls-concept:C1537677lld:lifeskim
pubmed-article:21868628lifeskim:mentionsumls-concept:C0376249lld:lifeskim
pubmed-article:21868628pubmed:issue6053lld:pubmed
pubmed-article:21868628pubmed:dateCreated2011-10-14lld:pubmed
pubmed-article:21868628pubmed:databankReferencehttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21868628pubmed:abstractTextUterine leiomyomas, or fibroids, are benign tumors that affect millions of women worldwide and that can cause considerable morbidity. To study the genetic basis of this tumor type, we examined 18 uterine leiomyomas derived from 17 different patients by exome sequencing and identified tumor-specific mutations in the mediator complex subunit 12 (MED12) gene in 10. Through analysis of 207 additional tumors, we determined that MED12 is altered in 70% (159 of 225) of tumors from a total of 80 patients. The Mediator complex is a 26-subunit transcriptional regulator that bridges DNA regulatory sequences to the RNA polymerase II initiation complex. All mutations resided in exon 2, suggesting that aberrant function of this region of MED12 contributes to tumorigenesis.lld:pubmed
pubmed-article:21868628pubmed:languageenglld:pubmed
pubmed-article:21868628pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21868628pubmed:citationSubsetIMlld:pubmed
pubmed-article:21868628pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21868628pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21868628pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21868628pubmed:statusMEDLINElld:pubmed
pubmed-article:21868628pubmed:monthOctlld:pubmed
pubmed-article:21868628pubmed:issn1095-9203lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:BöhlingTomTlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:YanJianJlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:LaunonenVirpi...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:AaltonenLauri...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:VahteristoPia...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:SjöbergJariJlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:TaipaleJussiJlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:GentileMassim...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:EngeMartinMlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:LehtonenHeli...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:TaipaleMinnaMlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:AavikkoMerviMlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:KoskiTaru ATAlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:KaasinenEeviElld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:TolvanenJaana...lld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:LiYilongYlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:MäkinenNettaNlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:MehineMiikaMlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:KatainenRikuRlld:pubmed
pubmed-article:21868628pubmed:authorpubmed-author:VirolainenEli...lld:pubmed
pubmed-article:21868628pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21868628pubmed:day14lld:pubmed
pubmed-article:21868628pubmed:volume334lld:pubmed
pubmed-article:21868628pubmed:ownerNLMlld:pubmed
pubmed-article:21868628pubmed:authorsCompleteYlld:pubmed
pubmed-article:21868628pubmed:pagination252-5lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:meshHeadingpubmed-meshheading:21868628...lld:pubmed
pubmed-article:21868628pubmed:year2011lld:pubmed
pubmed-article:21868628pubmed:articleTitleMED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas.lld:pubmed
pubmed-article:21868628pubmed:affiliationDepartment of Medical Genetics, Genome-Scale Biology Research Program, University of Helsinki, Helsinki, Finland.lld:pubmed
pubmed-article:21868628pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21868628pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
entrez-gene:9968entrezgene:pubmedpubmed-article:21868628lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:21868628lld:entrezgene