@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8> .
@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:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_head {
  this: np:hasAssertion dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_assertion;
    np:hasProvenance dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_provenance;
    np:hasPublicationInfo dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_assertion a np:Assertion .
  
  dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_provenance a np:Provenance .
  
  dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_assertion {
  miriam-gene:3283 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNeaa057b46d192f3b11168fd924946379 sio:SIO_000628 miriam-gene:3283, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_provenance {
  dgn-np:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_assertion dcterms:description
      "[Men with the variant genotypes at either B1-N367T or B2-c7519g had a significantly higher risk to develop prostate cancer, especially the hereditary type of prostate cancer. Most importantly, the subset of hereditary prostate cancer probands, whose families provided evidence for linkage at 1p13, predominantly contributed to the observed association. Additional studies are warranted to confirm these findings.]. 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:11912155;
    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:NP57496.RAdQeVYQO4LYQ-s7SlYjzW7tFPVSol3cF3x_K_wbULoR8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}