# OnCo record paper-barbieri-spop-foxa1-med12-prostate-nat-genet-2012 (paper). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)". Whole corpus: https://onco.cc/api/v1/onco.nt
@prefix schema: <https://schema.org/> .
@prefix onco: <https://onco.cc/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://onco.cc/key-papers/paper-barbieri-spop-foxa1-med12-prostate-nat-genet-2012/>
  a schema:ScholarlyArticle ;
  onco:kind "paper" ;
  schema:identifier "paper-barbieri-spop-foxa1-med12-prostate-nat-genet-2012" ;
  schema:name "Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer"@en ;
  schema:description "Sequencing the genes of 112 prostate cancers found the disease's commonest point mutation in a gene nobody had linked to it, and showed those tumours are a separate kind that never carries the usual fusion."@en ;
  schema:url <https://onco.cc/key-papers/paper-barbieri-spop-foxa1-med12-prostate-nat-genet-2012/> ;
  schema:dateModified "2026-09-25"^^xsd:date ;
  schema:citation <https://doi.org/10.1038/ng.2279>, <https://pubmed.ncbi.nlm.nih.gov/22610119/>, <https://www.cbioportal.org/study/summary?id=prad_broad> ;
  schema:sameAs <https://doi.org/10.1038/ng.2279> ;
  schema:datePublished "2012"^^xsd:gYear ;
  schema:author "Barbieri CE, Baca SC, Lawrence MS, et al." ;
  onco:cancers <https://onco.cc/cancers/prostate/> ;
  onco:technologies <https://onco.cc/technologies/wes-wgs/> ;
  onco:targets <https://onco.cc/targets/spop/>, <https://onco.cc/targets/foxa1/>, <https://onco.cc/targets/erg/> ;
  onco:pathways <https://onco.cc/pathways/ubiquitin-proteasome-system/>, <https://onco.cc/pathways/prostate-cancer-signalling/>, <https://onco.cc/pathways/ar-signaling/> ;
  onco:terms <https://onco.cc/terms/driver-mutation/>, <https://onco.cc/terms/gene-fusion/>, <https://onco.cc/terms/somatic-mutations-wxs-wgs/> ;
  onco:journals <https://onco.cc/journals/nature-genetics/> .