@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20> .
@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:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_head {
  this: np:hasAssertion dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_assertion;
    np:hasProvenance dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_provenance;
    np:hasPublicationInfo dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_assertion a np:Assertion .
  
  dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_provenance a np:Provenance .
  
  dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_assertion {
  miriam-gene:1282 a ncit:C16612 .
  
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    a sio:SIO_001121 .
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dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_provenance {
  dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_assertion dcterms:description
      "[With emphasis on cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), we review the molecular pathogenesis of recently characterized disorders including cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), retinal vasculopathy with cerebral leukodystrophy (RVCL) and the Collagen type IV, alpha 1 (COL4A1)-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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;
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dgn-np:NP748134.RAv-gJVWeaLw56KY_ZpMmKa9cCNpbb138vcG65PmTFf20130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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;
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