@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE> .
@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:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_head {
  this: np:hasAssertion dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_assertion;
    np:hasProvenance dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_provenance;
    np:hasPublicationInfo dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_assertion a np:Assertion .
  
  dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_provenance a np:Provenance .
  
  dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  
  lld:C0085413 a ncit:C7057 .
  
  dgn-gda:DGNe3992e47a8708c2c605a891d47683f71 sio:SIO_000628 miriam-gene:4846, lld:C0085413;
    a sio:SIO_001121 .
}

dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_provenance {
  dgn-np:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_assertion dcterms:description
      "[The demonstration of endothelial dysfunction in Pkd1(+/-) mice and ADPKD patients, and the effect of the frequent Glu298Asp polymorphism of ENOS on renal disease progression in ADPKD suggest that an impaired release of nitric oxide (NO) by endothelial cells can accelerate renal function degradation.]. 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:12832751;
    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:NP189291.RAVmqWoBwjVQvDYGTQ5fqWZTTOHZTj-6a9wPhjE4AjWiE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}