@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY> .
@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:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_head {
  this: np:hasAssertion dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_assertion;
    np:hasProvenance dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_provenance;
    np:hasPublicationInfo dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_assertion a np:Assertion .
  
  dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_provenance a np:Provenance .
  
  dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_assertion {
  miriam-gene:847 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNa729d84fdd93b776eec8ef791b5e68f3 sio:SIO_000628 miriam-gene:847, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_provenance {
  dgn-np:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_assertion dcterms:description
      "[This is the first study to implicate genetic variation in catalase in susceptibility to EHYT and suggests that polymorphisms in promoter regions may be particularly relevant to the study of complex diseases.]. 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:11479740;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP57660.RAANX0x9lWr_UUVcaJsFSDT5Zz3OyBpMhEvapqCme_iyY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:11+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" .
}