@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM> .
@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:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_head {
  this: np:hasAssertion dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_assertion;
    np:hasProvenance dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_provenance;
    np:hasPublicationInfo dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_assertion a np:Assertion .
  
  dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_provenance a np:Provenance .
  
  dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C2733225 a ncit:C7057 .
  
  dgn-gda:DGNa685ffde9de5416dcf13f3c9e18822d4 sio:SIO_000628 miriam-gene:3077, lld:C2733225;
    a sio:SIO_001121 .
}

dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_provenance {
  dgn-np:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_assertion dcterms:description
      "[The identification of mutations in the haemochromatosis gene (HFE) (C282Y and H63D) provides the unique opportunity to test whether genetic variants that are associated with tissue iron accumulation may influence the risk of coronary atherosclerosis.]. 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:10854101;
    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:NP331953.RAZpeeQ1TJQfTsPVyuVqVeiwsHMucnh7VUNPOk6swwLjM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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" .
}