@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw> .
@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:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_head {
  this: np:hasAssertion dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_assertion ;
    np:hasProvenance dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_provenance ;
    np:hasPublicationInfo dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_assertion a np:Assertion .
  dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_provenance a np:Provenance .
  dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  lld:C0023890 a ncit:C7057 .
  dgn-gda:DGN3d3e0d5c82e9673c6d487eb526592366 sio:SIO_000628 miriam-gene:3077 , lld:C0023890 ;
    a sio:SIO_001121 .
}
dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_provenance {
  dgn-np:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_assertion dcterms:description "[The aims of this study were to define the prevalence of the mutations 845G --> A and 187C --> G (C282Y and H63D) in the HFE gene associated with hereditary hemochromatosis in Italian patients with hepatocellular carcinoma occurring in cirrhosis and to analyze the interaction between these mutations and other established risk factors for hepatocellular carcinoma.]. 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:NP252116.RAraXiIgVsH_btyspmzGjqno6Pp7CDJXFLQ_g1DNhUeGw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}