@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic> .
@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:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_head {
  this: np:hasAssertion dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_assertion;
    np:hasProvenance dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_provenance;
    np:hasPublicationInfo dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_assertion a np:Assertion .
  
  dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_provenance a np:Provenance .
  
  dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0345904 a ncit:C7057 .
  
  dgn-gda:DGNce66b4b993f35aaedd28350176e594a2 sio:SIO_000628 miriam-gene:1565, lld:C0345904;
    a sio:SIO_001121 .
}

dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_provenance {
  dgn-np:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_assertion dcterms:description
      "[The frequency of CYP2D6 genes containing inactivating mutations was lower among 75 liver cancer patients than 200 healthy controls, and 40 cirrhotic subjects that did not develop liver cancer (frequency for carriers of two or more functional genes was 95% vs 74% vs 78%, respectively).]. 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:7898230;
    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:NP184551.RAXK1fJstTkEabrnYPXO0ZPnyeupUvf9gXT1nILNlpqic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:40+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" .
}