@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8> .
@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:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_head {
  this: np:hasAssertion dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion ;
    np:hasProvenance dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance ;
    np:hasPublicationInfo dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion a np:Assertion .
  dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance a np:Provenance .
  dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion {
  miriam-gene:6928 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGNaffb43a37da9430bd7eda8874feb1c93 sio:SIO_000628 miriam-gene:6928 , lld:C0376358 ;
    a sio:SIO_001122 .
}
dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_provenance {
  dgn-np:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_assertion dcterms:description "[We confirm recent reports that 8q24 variants identified to be associated with prostate cancer in men of European descent are also associated with prostate cancer in African Americans. Our report is the first to find evidence of association between SNPs near MSMB and prostate cancer in African Americans. Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been implicated to be independently associated, with respect to the widely reported SNP rs10993994 in the nearby gene MSMB, with prostate cancer in men of European descent.]. 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:20717903 ;
    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:NP67571.RAc1vV6F49sY-HoRwZAbvujiF-dREhFtfFHLxWfoJVaA8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}