@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI> .
@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:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_head {
  this: np:hasAssertion dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_assertion;
    np:hasProvenance dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_provenance;
    np:hasPublicationInfo dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_assertion a np:Assertion .
  
  dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_provenance a np:Provenance .
  
  dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_assertion {
  miriam-gene:4318 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN677f6f1308be924eb787d2609cf52aa9 sio:SIO_000628 miriam-gene:4318, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_provenance {
  dgn-np:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_assertion dcterms:description
      "[The joint analysis of the three MMP-9 polymorphisms, using logistical regression study did not reveal any statistically significant differences as far as the risk of developing prostate cancer is concerned based on the presence of the Q279R, P574R and -1562 C/T polymorphisms.]. 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:20354277;
    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:NP65772.RAzCac9jZbAn0-vOlt_DaN35TevaLihQ4BDM7iLqMteuI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}