@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo> .
@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:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_head {
  this: np:hasAssertion dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_assertion;
    np:hasProvenance dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_provenance;
    np:hasPublicationInfo dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_assertion a np:Assertion .
  
  dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_provenance a np:Provenance .
  
  dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_assertion {
  miriam-gene:3292 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGN446aaf6aa3ff65d55f768e7278170bab sio:SIO_000628 miriam-gene:3292, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_provenance {
  dgn-np:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_assertion dcterms:description
      "[We found no evidence that HSD17B1 htSNPs (including the nonsynonymous coding SNP S312G) or htSNP haplotypes were associated with risk of prostate cancer or tumor stage in the pooled multiethnic sample or in U.S. and European whites.]. 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:16311626;
    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:NP918367.RA3gBJATDAT2-qIAA_a7yDD7NtnEsR3xGzhSCroUDJBHo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}