@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ> .
@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/v4.0.0/void/> .

dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_head {
  this: np:hasAssertion dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_assertion;
    np:hasProvenance dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_provenance;
    np:hasPublicationInfo dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_assertion a np:Assertion .
  
  dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_provenance a np:Provenance .
  
  dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_assertion {
  miriam-gene:1571 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGNcfe03f77888496773d4256f471595559 sio:SIO_000628 miriam-gene:1571, lld:C0018801;
    a sio:SIO_001122 .
}

dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_provenance {
  dgn-np:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_assertion dcterms:description
      "[Knockdown or downregulation of CYP2E1 might be a therapeutic strategy to control the development of DCM after mutations of cTnT(R141W) or other factors, because DCM is the third most common cause of heart failure and the most frequent cause of heart transplantation.]. 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:22665122;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP987154.RArJVaY26dOUTEU-fq0hu_T0WGztMjuiogcLjSi_WuiAQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:12+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}