@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc> .
@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:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_head {
  this: np:hasAssertion dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_assertion;
    np:hasProvenance dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_provenance;
    np:hasPublicationInfo dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_assertion a np:Assertion .
  
  dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_provenance a np:Provenance .
  
  dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN7ef09b925ca37e301d7df4430aad61af sio:SIO_000628 miriam-gene:4524, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_provenance {
  dgn-np:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_assertion dcterms:description
      "[To assess the association and interaction of genotypic polymorphisms in MTHFR and lifestyle factors with prostate cancer in Taiwan, we investigated two well-known polymorphic variants of MTHFR, C677T (rs1801133) and A1298C (rs1801131), analyzed the association of specific genotypes with prostate cancer susceptibility, and discussed their joint effects with individual habits on prostate cancer risk.]. 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:20944139;
    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:NP69477.RA_BB6EQ7U5OgPdVaYShWhQ7ek1kVxhRJtUwXrglk8DBc130_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>;
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}