@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0> .
@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:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_head {
  this: np:hasAssertion dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_assertion;
    np:hasProvenance dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_provenance;
    np:hasPublicationInfo dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_assertion a np:Assertion .
  
  dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_provenance a np:Provenance .
  
  dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_assertion {
  miriam-gene:2395 a ncit:C16612 .
  
  lld:C0282193 a ncit:C7057 .
  
  dgn-gda:DGNcc97eaa4967b70a5bc779e9a4b589d86 sio:SIO_000628 miriam-gene:2395, lld:C0282193;
    a sio:SIO_001121 .
}

dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_provenance {
  dgn-np:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_assertion dcterms:description
      "[This chapter considers the most common inherited disorder in individuals of European ancestry (hereditary hemochromatosis), a widespread disease in sub-Saharan populations for which the genetic basis is still uncertain (African dietary iron overload), and several less frequent or rare disorders (juvenile hemochromatosis, atransferrinemia, aceruloplasminemia, hyperferritinemia with autosomal dominant congenital cataract, Friedreich's ataxia, and X-linked sideroblastic anemia with ataxia).]. 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:10774476;
    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:NP413726.RA_EXMGoT21qWIPfLJdYPr5KY6clFvQcnM7awGKO9DBe0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:05+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" .
}