@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU> .
@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:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_head {
  this: np:hasAssertion dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion;
    np:hasProvenance dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance;
    np:hasPublicationInfo dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion a np:Assertion .
  
  dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance a np:Provenance .
  
  dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0002874 a ncit:C7057 .
  
  dgn-gda:DGNb9f67808e9943c4162878ef792db3536 sio:SIO_000628 miriam-gene:3077, lld:C0002874;
    a sio:SIO_001122 .
}

dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_provenance {
  dgn-np:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_assertion dcterms:description
      "[It seems that MDS and AA patients are susceptible to iron overload, in the diseases itself and the mutations of HFE gene are not the major factor for iron overload in the patients.]. 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:19731820;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP73782.RAwEBW-5Uv-TQO4ZRfX2yeMVzskU-pc8LPekZtiG11RpU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}