@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw> .
@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/v4.0.0/void/> .

dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_head {
  this: np:hasAssertion dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_assertion;
    np:hasProvenance dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_provenance;
    np:hasPublicationInfo dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_assertion a np:Assertion .
  
  dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_provenance a np:Provenance .
  
  dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGNd90086919b995e1dbb3ca13b8f144b52 sio:SIO_000628 miriam-gene:3077, lld:C0282193;
    a sio:SIO_001121 .
}

dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_provenance {
  dgn-np:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_assertion dcterms:description
      "[We show that in this family the mutation which is fully penetrant, may act through an increased iron export from macrophages as suggested by the unexpected absence of iron overload in the spleen and bone marrow detected by magnetic resonance imaging, that it co-segregates with a phenotype close to the classical form of HFE-associated hemochromatosis and was associated, in the oldest patient, with the development of hepatocellular carcinoma in a non cirrhotic liver.]. 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:18403150;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP665138.RAZVxbYMFahKbzAHQRYNnoGb2AoeRdtQ5j9g78I_06vhw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:47+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}