@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM> .
@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:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_head {
  this: np:hasAssertion dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion;
    np:hasProvenance dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance;
    np:hasPublicationInfo dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion a np:Assertion .
  
  dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance a np:Provenance .
  
  dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion {
  miriam-gene:3769 a ncit:C16612 .
  
  lld:C3272363 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_provenance {
  dgn-np:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_assertion dcterms:description
      "[For the first time to our knowledge, we report this association not only for LVD and SVD but also for cryptogenic stroke, implying that future studies of the genetics of ischemic stroke should target these 3 subtypes.]. 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:15933254;
    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:NP591864.RAg7z9hbUK3DrxtPJVbplbRz6CQt9WFnqicF7Dk87GEcM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}