@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c> .
@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:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_head {
  this: np:hasAssertion dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion;
    np:hasProvenance dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance;
    np:hasPublicationInfo dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion a np:Assertion .
  
  dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance a np:Provenance .
  
  dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGNca7eaf63b263fe02d1b3a28297c429cd sio:SIO_000628 miriam-gene:348, lld:C0282193;
    a sio:SIO_001121 .
}

dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_provenance {
  dgn-np:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_assertion dcterms:description
      "[In this pilot study, common variants of the apolipoprotein E (APOE) and HFE genes resulting in the iron overload disorder of hereditary hemochromatosis (C282Y, H63D and S65C) were evaluated as factors in sporadic AD in an Ontario sample in which folic acid fortification has been mandatory since 1998.]. 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:18525129;
    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:NP571107.RA5hIryjot5nGC8Q9pdCgl8XQecizgOO5K1aiklDPwV0c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:44+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" .
}