@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM> .
@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:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_head {
  this: np:hasAssertion dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion;
    np:hasProvenance dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance;
    np:hasPublicationInfo dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion a np:Assertion .
  
  dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance a np:Provenance .
  
  dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C2733158 a ncit:C7057 .
  
  dgn-gda:DGNfea69c032841e14334f4b2411dd3a70e sio:SIO_000628 miriam-gene:5972, lld:C2733158;
    a sio:SIO_001121 .
}

dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_provenance {
  dgn-np:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_assertion dcterms:description
      "[Genetic association studies in the setting of the Austrian Stroke Prevention Study described that polymorphisms in the renin angiotensin system (RAS) increase the susceptibility for progression of cerebral small vessel disease.]. 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:12456049;
    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:NP856448.RARLGkoPM_gvYHCDYKG8Pyj9hMZFK91iXgT8uqY0W17SM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}