@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g> .
@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:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_head {
  this: np:hasAssertion dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_assertion;
    np:hasProvenance dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_provenance;
    np:hasPublicationInfo dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_assertion a np:Assertion .
  
  dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_provenance a np:Provenance .
  
  dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_assertion {
  miriam-gene:3483 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN3155af987f59eb4572ff90c4633310a7 sio:SIO_000628 miriam-gene:3483, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_provenance {
  dgn-np:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_assertion dcterms:description
      "[Eleven haplotype tagging SNPs and two single SNPs in the IGFBP1, IGFBP3, and IGFALS genes were genotyped within the CAncer Prostate in Sweden (CAPS) study including 2,774 cases and 1,736 controls.]. 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:19455605;
    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:NP72882.RAUWFrWfKEpG-TB9-2nholKAM_0ZPZRyeFXah5daYqC_g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}