@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_head {
   this: np:hasAssertion dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_assertion ;
    np:hasProvenance dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_provenance ;
    np:hasPublicationInfo dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_assertion a np:Assertion .
  dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_provenance a np:Provenance .
  dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_assertion {
   miriam-gene:10499 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGN6eb74cf299e7e1d24405e420caba34bd sio:SIO_000628 miriam-gene:10499 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_provenance {
   dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_assertion dcterms:description "[We sequenced the coding exons of 17 genes (EP300, CCND1, NME1, NCOA1, NCOA2, NCOA3, SMARCA4, SMARCA2, CARM1, FOXA1, MPG, NCOR1, NCOR2, CALCOCO1, PRMT1, PPARBP and CREBBP) suggested to influence transcriptional activation by steroid hormone receptors in a multiethnic panel of women with advanced breast cancer (n = 95): African Americans, Latinos, Japanese, Native Hawaiians and European Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:19183483 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP69128.RAvFhUJZrIS4M6g8FKl7ndsAO-Ly4O0WguzScQrXMrdiI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:33+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}