@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U> .
@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:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_head {
  this: np:hasAssertion dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion;
    np:hasProvenance dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance;
    np:hasPublicationInfo dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion a np:Assertion .
  
  dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance a np:Provenance .
  
  dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGNd847dcad4de562df3750f712d995016f sio:SIO_000628 miriam-gene:3077, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_provenance {
  dgn-np:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_assertion dcterms:description
      "[At the cellular level, the HFE mutant protein resulting from the H63D HFE gene variant is associated with iron dyshomeostasis, increased oxidative stress, glutamate release, tau phosphorylation, and alteration in inflammatory response, each of which is under investigation as a contributing factor to neurodegenerative 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:21346098;
    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:NP574757.RAtV3S5GE2NL5DThvPLzzbKypQThtRVWwHdvH4yxrYg5U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:46+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" .
}