@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_head {
  this: np:hasAssertion dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion;
    np:hasProvenance dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance;
    np:hasPublicationInfo dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion a np:Assertion .
  
  dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance a np:Provenance .
  
  dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0018995 a ncit:C7057 .
  
  dgn-gda:DGN8d4e7592a882a6139c5b8cef2839ad9a sio:SIO_000628 miriam-gene:3077, lld:C0018995;
    a sio:SIO_001122 .
}

dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_provenance {
  dgn-np:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_assertion dcterms:description
      "[study of H63D homozygotes supports the conclusion that this genotype must be taken into account, because it confers an increased risk of iron overload and genetic susceptibility to developing hereditary hemochromatosis or to aggravating other diseases ]. 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:16364490;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP214695.RAtR18s6SeJz4TARSRak19dSLe-E0LB_HB2nFwQUjq9sY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:24+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}