@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM> .
@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/v3.0.0/void/> .

dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_head {
  this: np:hasAssertion dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_assertion;
    np:hasProvenance dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_provenance;
    np:hasPublicationInfo dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_assertion a np:Assertion .
  
  dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_provenance a np:Provenance .
  
  dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_assertion {
  miriam-gene:6648 a ncit:C16612 .
  
  lld:C0878544 a ncit:C7057 .
  
  dgn-gda:DGN4f912a579d49952e3be2ae34d34c4bda sio:SIO_000628 miriam-gene:6648, lld:C0878544;
    a sio:SIO_001121 .
}

dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_provenance {
  dgn-np:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_assertion dcterms:description
      "[In patients with hereditary haemochromatosis, the MnSOD genotype affects the risk of cardiomyopathy related to iron overload and possibly to other known and unknown risk factors and could represent an iron toxicity modifier gene.]. 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:15591282;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP707120.RAmn2GbxMPCuxLyzIkPvvl3kimL5F7tTy_HeuS7BDrbvM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:46+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}