@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI> .
@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:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_head {
  this: np:hasAssertion dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion;
    np:hasProvenance dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance;
    np:hasPublicationInfo dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion a np:Assertion .
  
  dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance a np:Provenance .
  
  dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion {
  miriam-gene:4683 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN5c9012879092c58fcedb2b9d3f3e6873 sio:SIO_000628 miriam-gene:4683, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_provenance {
  dgn-np:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_assertion dcterms:description
      "[These findings suggest that heterozygous carriers of the NBS1 founder mutation exhibit increased susceptibility to prostate cancer and that the cancers that develop in the prostates of carriers are functionally homozygous for the mutation.]. 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:14973119;
    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:NP53983.RArZPPhX42BQkPlH-t_2wjo1hL1omwAeXBTiCw1_29vPI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}