@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s> .
@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:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_head {
  this: np:hasAssertion dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_assertion;
    np:hasProvenance dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_provenance;
    np:hasPublicationInfo dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_assertion a np:Assertion .
  
  dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_provenance a np:Provenance .
  
  dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNb413187234fc020d6ae295ec8a6be4c2 sio:SIO_000628 miriam-gene:3077, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_provenance {
  dgn-np:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_assertion dcterms:description
      "[Aims of the study were: (i) to determine the prevalence of mutations C282Y and H63D in the HFE gene causing hereditary hemochromatosis in patients with type 2 diabetes mellitus and non-diabetics, (ii) to investigate the relationship among HFE genotypes, serum ferritin and glucose intolerance and (iii) to assess possible association of HFE mutations with the susceptibility to develop late diabetic complications in the Czech population.]. 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:12148086;
    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:NP508544.RArwEc037PGS5KNzY7BAJ0ox3fW3EpcofVfd4M7BvYj4s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:03+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" .
}