@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg> .
@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:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_head {
  this: np:hasAssertion dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_assertion;
    np:hasProvenance dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_provenance;
    np:hasPublicationInfo dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_assertion a np:Assertion .
  
  dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_provenance a np:Provenance .
  
  dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0392514 a ncit:C7057 .
  
  dgn-gda:DGNdb978f4ccd0e833b057462d6f80be547 sio:SIO_000628 miriam-gene:3077, lld:C0392514;
    a sio:SIO_001121 .
}

dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_provenance {
  dgn-np:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_assertion dcterms:description
      "[The description of two mutations in the HFE gene (Cys282Tyr and His63Asp) related to hereditary hemochromatosis provides an opportunity to address the question of the association between iron overload and atherosclerosis.]. 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:10719381;
    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:NP164926.RAC9ijWzKKuBQzOa6Mn7qSv11cWyetnKssNIU_ApKGCDg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}