@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s> .
@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:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_head {
  this: np:hasAssertion dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion;
    np:hasProvenance dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance;
    np:hasPublicationInfo dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion a np:Assertion .
  
  dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance a np:Provenance .
  
  dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion {
  miriam-gene:1586 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGNab190a5fdd4b2f78cfa199ab6c81cf23 sio:SIO_000628 miriam-gene:1586, lld:C0023895;
    a sio:SIO_001122 .
}

dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_provenance {
  dgn-np:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_assertion dcterms:description
      "[Our study provides the first evidence that CYP17 polymorphism participates in the development of THS, and sheds light on the genetic causes of this side effect and genetic differences between tamoxifen-treated individuals.]. 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:15706422;
    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:NP63162.RAa2J-s8eIcy6sgqihJmQNbytnaQudhde5aVeyMUcSi5s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}