@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk> .
@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:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_head {
  this: np:hasAssertion dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion;
    np:hasProvenance dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance;
    np:hasPublicationInfo dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion a np:Assertion .
  
  dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance a np:Provenance .
  
  dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0023890 a ncit:C7057 .
  
  dgn-gda:DGNc08abada5df43fe0b2080b135ae56e51 sio:SIO_000628 miriam-gene:3077, lld:C0023890;
    a sio:SIO_001121 .
}

dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_provenance {
  dgn-np:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_assertion dcterms:description
      "[Then, the type of liver siderosis (parenchymal, mesenchymal or mixed) and its distribution throughout the lobule and the liver are useful means for suggesting its etiology: HLA-linked hemochromatosis gene (HFE) hemochromatosis or other rare genetic hemochromatosis, nonhemochromatotic genetic iron overload (ferroportin disease, aceruloplasminemia), or iron overload secondary to excessive iron supply, inflammatory syndrome, noncirrhotic chronic liver diseases including dysmetabolic iron overload syndrome, cirrhosis, and blood disorders.]. 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:17729397;
    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:NP171811.RAqPbQzi4AfgPPiaz9z0CBlx6bky4j952eTRpG9uk6ITk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}