@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE> .
@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:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_head {
  this: np:hasAssertion dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_assertion;
    np:hasProvenance dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_provenance;
    np:hasPublicationInfo dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_assertion a np:Assertion .
  
  dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_provenance a np:Provenance .
  
  dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  
  lld:C0270612 a ncit:C7057 .
  
  dgn-gda:DGN59e0a844f3a14694a02301525a68981e sio:SIO_000628 miriam-gene:4854, lld:C0270612;
    a sio:SIO_001121 .
}

dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_provenance {
  dgn-np:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_assertion dcterms:description
      "[Therefore, we propose to consider a replacement for the name CADASIL that better reflects the morphological picture of the disease like, for example, cerebral autosomal dominant vasculopathy with subcortical infarcts and leukoencephalopathy (CADVaSIL) or, to preserve the commonly known acronym, cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.]. 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:15068168;
    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:NP367752.RAo8OmhzInB29GSokaPIgro5jEDmKdimwCLBBs9aSWUPE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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" .
}