@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A> .
@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:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_head {
  this: np:hasAssertion dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion;
    np:hasProvenance dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance;
    np:hasPublicationInfo dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion a np:Assertion .
  
  dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance a np:Provenance .
  
  dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion {
  miriam-gene:5627 a ncit:C16612 .
  
  lld:C0600139 a ncit:C7057 .
  
  dgn-gda:DGN755e075191fdab150c1d6820c72a5f20 sio:SIO_000628 miriam-gene:5627, lld:C0600139;
    a sio:SIO_001121 .
}

dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_provenance {
  dgn-np:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_assertion dcterms:description
      "[We therefore studied VDR gene polymorphisms, as detected by Apal and Taql restriction fragments, in multiethnic Brazilian men (165 patients and 200 controls) for association with prostate cancer risk and parameters of disease severity (serum PSA, Gleason score and tumor stage).]. 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:15503828;
    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:NP178885.RAdPwVyrF15MuP-o0KTxOfK-K2nj2qqBwZZMQfaWUc98A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}