@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM> .
@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:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_head {
  this: np:hasAssertion dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion;
    np:hasProvenance dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance;
    np:hasPublicationInfo dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion a np:Assertion .
  
  dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance a np:Provenance .
  
  dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN4974e23083a58741f1cadb6a6d4982a7 sio:SIO_000628 miriam-gene:672, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_provenance {
  dgn-np:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_assertion dc:description
      "[To establish whether or not inherited variation in BRCA1 influences prostate cancer risk we genotyped 1793 men with prostate cancer in Poland and 4570 controls for three founder mutations (C61G, 4153delA and 5382insC).]. 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:18090912;
    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:NP81508.RAb1i3KoexWFwiTLPuc8BmFSFCOkrON4jajzZm_1wzhOM130_publicationInfo {
  this: dc:created "2014-10-02T12:32:40+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}