@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ> .
@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:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_head {
  this: np:hasAssertion dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_assertion;
    np:hasProvenance dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_assertion a np:Assertion .
  
  dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_provenance a np:Provenance .
  
  dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGN2664d3f1dae409fecd311ccead8bff7c sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001122 .
}

dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_provenance {
  dgn-np:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_assertion dcterms:description
      "[The Hemochromatosis and Iron Overload Screening (HEIRS) Study screened 101,168 primary care participants for iron overload with serum transferrin saturation (TS), ferritin, and C282Y and H63D mutations of the HFE gene.]. 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:16797244;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP556339.RA4EXrGe5-_7F7K-36BdHmRrNbVlkQ-AFZG0jQWRa6XFQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:57+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" .
}