@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_head {
  this: np:hasAssertion dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_assertion;
    np:hasProvenance dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_provenance;
    np:hasPublicationInfo dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_assertion a np:Assertion .
  
  dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_provenance a np:Provenance .
  
  dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_assertion {
  miriam-gene:6928 a ncit:C16612 .
  
  lld:C1306459 a ncit:C7057 .
  
  dgn-gda:DGN7cd706d0506da8ebde846a5fa542b4a2 sio:SIO_000628 miriam-gene:6928, lld:C1306459;
    a sio:SIO_001121 .
}

dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_provenance {
  dgn-np:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_assertion dcterms:description
      "[To fine-map common genetic variation in this region, we genotyped 79 single nucleotide polymorphisms (SNPs) in the 17q12 region harboring HNF1B in 10 272 prostate cancer cases and 9123 controls of European ancestry from 10 case-control studies as part of the Cancer Genetic Markers of Susceptibility (CGEMS) initiative.]. 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:21576123;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP725154.RAvR56RSF1idatCTfydBxV2WaLtWqAdG9FgFTCpELWMPQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:57+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}