@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg> .
@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:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_head {
  this: np:hasAssertion dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_assertion;
    np:hasProvenance dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_provenance;
    np:hasPublicationInfo dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_assertion a np:Assertion .
  
  dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_provenance a np:Provenance .
  
  dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN619eb0b6222559edf516bcb0a24e99d9 sio:SIO_000628 miriam-gene:5663, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_provenance {
  dgn-np:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_assertion dcterms:description
      "[We further show that brains and primary neuronal cultures from Ets2 transgenic mice, as well as 3T3 fibroblasts that overexpress ETS2, display molecular abnormalities also seen in DS, such as elevated expression of beta-APP protein, an increase in presenilin-1 and increased beta-amyloid production.]. 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:12890557;
    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:NP198399.RAWiENiDVNow7DdYkG4s50vIcszJ__DG_inWig8T_Pmcg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}