@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA> .
@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:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_head {
  this: np:hasAssertion dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion;
    np:hasProvenance dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance;
    np:hasPublicationInfo dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion a np:Assertion .
  
  dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance a np:Provenance .
  
  dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0009088 a ncit:C7057 .
  
  dgn-gda:DGN73514d4955e56970443778c77e2dfb40 sio:SIO_000628 miriam-gene:3077, lld:C0009088;
    a sio:SIO_001121 .
}

dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_provenance {
  dgn-np:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_assertion dcterms:description
      "[A 60-year-old woman with secondary chronic cluster headache had increased serum ferritin and serum transferrin saturation and was homozygous for the C282Y mutation in the HFE gene, which is indicative of hereditary haemochromatosis.]. 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:12100096;
    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:NP874345.RAKYXtY-q_yOoGxdUlMe04Zqi4clKumViSfaT8cV921kA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}