@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI> .
@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:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_head {
  this: np:hasAssertion dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_assertion;
    np:hasProvenance dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_provenance;
    np:hasPublicationInfo dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_assertion a np:Assertion .
  
  dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_provenance a np:Provenance .
  
  dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_assertion {
  miriam-gene:1499 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGN6322c1076154d9b91e026540a456f396 sio:SIO_000628 miriam-gene:1499, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_provenance {
  dgn-np:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_assertion dcterms:description
      "[We comprehensively studied the contribution of genetic variations in CTNNB1 and adenomatous polyposis coli (APC), one of the key genes encoding the CTNNB1 destruction complex, to PCa risk and prognosis after RP using a hospital-based case-control study.]. 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:19777185;
    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:NP416810.RAa-hPb28ly2YWci_paD0nMVd0jUs3xAN53h4MW_zoJZI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:07+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" .
}