@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw> .
@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:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_head {
  this: np:hasAssertion dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_assertion;
    np:hasProvenance dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_provenance;
    np:hasPublicationInfo dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_assertion a np:Assertion .
  
  dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_provenance a np:Provenance .
  
  dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGN4ca1b6b00bdc9145664fafe6932fc986 sio:SIO_000628 miriam-gene:3077, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_provenance {
  dgn-np:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_assertion dcterms:description
      "[In this article, the incidence and prevalence of HCC in patients with HH and other liver diseases associated with iron overload are discussed as well as the possible mechanisms for the increased risk for hepatic carcinogenesis in these disorders.]. 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:15508107;
    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:NP709753.RAkPT-aIYfsXp3IDzfeV-tJk5Hsmm8g47ElHz_egO2OIw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}