@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ> .
@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:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_head {
  this: np:hasAssertion dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion;
    np:hasProvenance dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance;
    np:hasPublicationInfo dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion a np:Assertion .
  
  dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance a np:Provenance .
  
  dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion {
  miriam-gene:79017 a ncit:C16612 .
  
  lld:C1457883 a ncit:C7057 .
  
  dgn-gda:DGN198e0d95dcd179f82207e995357e76c4 sio:SIO_000628 miriam-gene:79017, lld:C1457883;
    a sio:SIO_001121 .
}

dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_provenance {
  dgn-np:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_assertion dcterms:description
      "[The prostate is an androgen-regulated organ and polymorphisms in genes involved in testosterone synthesis, in particular, SRD5A2 (A49T and V89L variants), CYP17 (MspAI variant), and the AR (CAG, GGC repeats), represent candidate risk factors for prostate cancer incidence and aggressiveness.]. 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:14991867;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP641157.RAn_S6AAcnBZPyeoLm1xlWINFPPeWrSDa7_iDzrpCRJxQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}