@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE> .
@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 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:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_head {
  this: np:hasAssertion dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_assertion;
    np:hasProvenance dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_provenance;
    np:hasPublicationInfo dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_assertion a np:Assertion .
  
  dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_provenance a np:Provenance .
  
  dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_assertion {
  miriam-gene:11200 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGNb56a607774414931454016f3a8d330d2 sio:SIO_000628 miriam-gene:11200, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_provenance {
  dgn-np:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_assertion dct:description
      "[These results suggest that testing for germline CHEK2 mutations improves the ability to predict the presence of prostate cancer in screened men, however, the clinical utility of incorporating DNA variants in the screening process is marginal.]. 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:23722471;
    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:NP361428.RAAqFmUwT8UeOXuhCQODLEn7MvL62rUZyKEjc30bK0wgE130_publicationInfo {
  this: dct:created "2014-10-02T12:35:32+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}