@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw> .
@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:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_head {
  this: np:hasAssertion dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_assertion;
    np:hasProvenance dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_provenance;
    np:hasPublicationInfo dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_assertion a np:Assertion .
  
  dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_provenance a np:Provenance .
  
  dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0038525 a ncit:C7057 .
  
  dgn-gda:DGN7eee25e57a23bc7a36dfc39531a1edf2 sio:SIO_000628 miriam-gene:183, lld:C0038525;
    a sio:SIO_001121 .
}

dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_provenance {
  dgn-np:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_assertion dcterms:description
      "[The combination of Sox17 deficiency and angiotensin II infusion in mice induces vascular abnormalities closely resembling the cardinal features of IA such as luminal dilation, wall thinning, tortuosity, and subarachnoid hemorrhages.]. 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:25596186;
    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:NP1256216.RAsCqXFz1LGw_VctXuyDNZg9eHrYJngPcmdPfCfeaEsxw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:15+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" .
}