@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw> .
@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/v3.0.0/void/> .

dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_head {
  this: np:hasAssertion dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_assertion;
    np:hasProvenance dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_provenance;
    np:hasPublicationInfo dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_assertion a np:Assertion .
  
  dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_provenance a np:Provenance .
  
  dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  
  lld:C3272363 a ncit:C7057 .
  
  dgn-gda:DGN13fd0d27c19a76480967a12ce40c02cf sio:SIO_000628 miriam-gene:4854, lld:C3272363;
    a sio:SIO_001121 .
}

dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_provenance {
  dgn-np:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_assertion dcterms:description
      "[To investigate the Notch 3 mutation spectrum in Arab patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy CADASIL, which is an inherited cerebrovascular disease characterized by recurrent subcortical ischemic stroke starting in the third or fourth decade.]. 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:18626519;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP596657.RAB5edezpFDbxT9G2Jb_PEjiAbpnk8XTxdeaBjZFX9OWw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:36+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}