@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_head {
   this: np:hasAssertion dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_assertion ;
    np:hasProvenance dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_provenance ;
    np:hasPublicationInfo dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_assertion a np:Assertion .
  dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_provenance a np:Provenance .
  dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_assertion {
   miriam-gene:4854 a ncit:C16612 .
  lld:C0149931 a ncit:C7057 .
  dgn-gda:DGNeb9e420764a0ab6a23d6c3fe8f8381ab sio:SIO_000628 miriam-gene:4854 , lld:C0149931 ;
    a sio:SIO_001121 .
}
dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_provenance {
   dgn-np:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_assertion dcterms:description "[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene and is clinically characterized by recurrent stroke, cognitive decline, psychiatric disturbances and migraine.]. 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:21038489 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP849460.RAY52X1i5pkufyHQV0CqvNJ2O95Ng1slbk13epZ9Rf8NI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:09+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}