@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10> .
@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:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_head {
  this: np:hasAssertion dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion ;
    np:hasProvenance dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance ;
    np:hasPublicationInfo dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion a np:Assertion .
  dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance a np:Provenance .
  dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  lld:C0497327 a ncit:C7057 .
  dgn-gda:DGN97f72f2ed2c610f10de62a1616a66824 sio:SIO_000628 miriam-gene:4854 , lld:C0497327 ;
    a sio:SIO_001121 .
}
dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_provenance {
  dgn-np:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_assertion dcterms:description "[Mutations in the human Notch 3 gene cause the vascular stroke and dementia syndrome CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) characterized by degeneration of vascular smooth muscle cells and multiple small infarcts in the white and deep gray matter of the brain.]. 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:12126955 ;
    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:NP492550.RAgWbTgoA79X-0UMz3hA8vwGpt5tqIY9ppkAFgJnyqs10130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:54+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" .
}