@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0> .
@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 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:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_head {
  this: np:hasAssertion dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion;
    np:hasProvenance dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance;
    np:hasPublicationInfo dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion a np:Assertion .
  
  dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance a np:Provenance .
  
  dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion {
  miriam-gene:2162 a ncit:C16612 .
  
  lld:C0948008 a ncit:C7057 .
  
  dgn-gda:DGN6760f4216477306f84131d58ceda3edd sio:SIO_000628 miriam-gene:2162, lld:C0948008;
    a sio:SIO_001122 .
}

dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_provenance {
  dgn-np:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_assertion dct:description
      "[There is a genetic component to common stroke. No single gene with major effect was identified; rather, common variants in several genes, each exerting a modest effect, contribute to the risk of stroke. These findings have important implications for the design of future genetic studies and for predictive genetic testing for stroke and other multifactorial diseases.]. 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:15534175;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44618.RAuwNKSeN1CHYjgKD8LRNwSbeOa0qU1Tv0t1zSZWOS0I0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}