@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII> .
@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/v3.0.0/void/> .

dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_head {
  this: np:hasAssertion dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_assertion;
    np:hasProvenance dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_provenance;
    np:hasPublicationInfo dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_assertion a np:Assertion .
  
  dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_provenance a np:Provenance .
  
  dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0009088 a ncit:C7057 .
  
  dgn-gda:DGN2232209c4af3a721db56bcfb38b518d3 sio:SIO_000628 miriam-gene:3077, lld:C0009088;
    a sio:SIO_001122 .
}

dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_provenance {
  dgn-np:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP446753.RAeM7G7dWOLaTyY-UDycVBQ9Mcr1f4jIq6L3qzKwczPII130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:02+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}