@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo> .
@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:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_head {
  this: np:hasAssertion dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_assertion;
    np:hasProvenance dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_provenance;
    np:hasPublicationInfo dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_assertion a np:Assertion .
  
  dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_provenance a np:Provenance .
  
  dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C1623038 a ncit:C7057 .
  
  dgn-gda:DGN1e865f4b56c27c7054eda1fad312becd sio:SIO_000628 miriam-gene:3077, lld:C1623038;
    a sio:SIO_001121 .
}

dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_provenance {
  dgn-np:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_assertion dcterms:description
      "[It is less well established that the prevalence of the HFE mutations is increased in alcoholic liver disease and in chronic viral hepatitis, but in both conditions, patients harboring one of these mutations, especially C282Y, are more likely to have advanced hepatic fibrosis or cirrhosis.]. 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:10980924;
    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:NP207045.RApu5aS6Gr_sFSdrDlS6mpEiXLHtkBf2FRW7C3bMcuxLo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+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" .
}