@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo> .
@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:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_head {
  this: np:hasAssertion dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_assertion;
    np:hasProvenance dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_provenance;
    np:hasPublicationInfo dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_assertion a np:Assertion .
  
  dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_provenance a np:Provenance .
  
  dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0279000 a ncit:C7057 .
  
  dgn-gda:DGN157dcfd7e91ca611b32b15d9131bcbb8 sio:SIO_000628 miriam-gene:3077, lld:C0279000;
    a sio:SIO_001121 .
}

dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_provenance {
  dgn-np:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_assertion dcterms:description
      "[These data indicate that the prevalence of the main mutation associated with hereditary hemochromatosis is significantly higher in cirrhotic Italian patients with hepatocellular carcinoma compared to a normal population and suggest that heterozygotes for HFE mutations exposed to hepatitis virus infections or who had been alcohol abusers could have an increased risk of developing cirrhosis and later liver cancer than people without the mutations exposed to the same risk factors.]. 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:11500061;
    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:NP426224.RAjYVDlxcS2LE8n2FPcFwg6ZIUUQvlHc6boDVZ26GreEo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}