@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI> .
@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:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_head {
  this: np:hasAssertion dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion;
    np:hasProvenance dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance;
    np:hasPublicationInfo dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion a np:Assertion .
  
  dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance a np:Provenance .
  
  dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion {
  miriam-gene:11093 a ncit:C16612 .
  
  lld:C0398623 a ncit:C7057 .
  
  dgn-gda:DGN6d681d24a874bbe3908a18533e35016e sio:SIO_000628 miriam-gene:11093, lld:C0398623;
    a sio:SIO_001121 .
}

dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_provenance {
  dgn-np:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_assertion dcterms:description
      "[Recent studies have shown that increased plasma levels of Von Willebrand factor (VWF) and reduced plasma levels of enzyme ADAMTS13 are associated with diabetic nephropathy and an increased risk of developing cardiovascular disease, suggesting that these markers of hypercoagulability may contribute to an increased risk of cardiovascular disease in diabetic patients with impaired renal function.]. 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:23159842;
    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:NP434008.RAAGzqFOGVaEPDrI9pvAeGGNPhYTpsWfEKy7oRKDkVpbI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:17+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" .
}