@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc> .
@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:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_head {
  this: np:hasAssertion dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion;
    np:hasProvenance dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance;
    np:hasPublicationInfo dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion a np:Assertion .
  
  dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance a np:Provenance .
  
  dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion {
  miriam-gene:4855 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN05e62725ded95588e002325218ec2885 sio:SIO_000628 miriam-gene:4855, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance {
  dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion dcterms:description
      "[We directly sequenced all 33 exons, the promoter and 3'-untranslated region of NOTCH3 in 195 participants with either coalescent white matter lesions or lacunes and compared the results to 82 randomly selected participants with no focal changes on magnetic resonance images in the Austrian Stroke Prevention Study.]. 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:22006983;
    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:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}