@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk> .
@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 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:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_head {
  this: np:hasAssertion dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion ;
    np:hasProvenance dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance ;
    np:hasPublicationInfo dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion a np:Assertion .
  dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance a np:Provenance .
  dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion {
  miriam-gene:367 a ncit:C16612 .
  lld:C0376358 a ncit:C7057 .
  dgn-gda:DGN0adb4cf9e72593c2316220599e4f927d sio:SIO_000628 miriam-gene:367 , lld:C0376358 ;
    a sio:SIO_001122 .
}
dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_provenance {
  dgn-np:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_assertion dct:description "[The purpose of this study was to analyse the frequency and type of mutations in the coding region of androgen receptor (AR) and to determine the role of polymorphisms in the intron 1 of ERalpha, exon 5 of ERbeta, intron 7 of progesterone, exon 7 of the aromatase (CYP19) and exon 9 of VDR genes in the risk of prostate cancer.]. 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:18483761 ;
    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:NP48023.RAoZFfJd048BDh3RBaQNVnodAKTIjq5koXGTjvU5wtVnk130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}