@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk> .
@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:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_head {
  this: np:hasAssertion dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_assertion ;
    np:hasProvenance dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_provenance ;
    np:hasPublicationInfo dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_assertion a np:Assertion .
  dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_provenance a np:Provenance .
  dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_assertion {
  miriam-gene:4854 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGN8c9e8c6cfa73df79e43e9a182c829852 sio:SIO_000628 miriam-gene:4854 , lld:C0038454 ;
    a sio:SIO_001122 .
}
dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_provenance {
  dgn-np:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_assertion dcterms:description "[To gain insight into how Notch 3 function is linked to CADASIL pathophysiology, we studied two phenotypically distinct mutations, C455R and R1031C, respectively associated with early and late onset of stroke, by using hemodynamic analyses in transgenic mouse models, receptor activity assays in cell culture, and proteomic examination of postmortem human tissue.]. 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:21555590 ;
    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:NP892713.RAPme6SkBhgGeykHf9KFTqZXzIr7Knjcu9drCaRz1EHBk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:29+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" .
}