@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc> .
@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:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_head {
  this: np:hasAssertion dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_assertion;
    np:hasProvenance dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_provenance;
    np:hasPublicationInfo dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_assertion a np:Assertion .
  
  dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_provenance a np:Provenance .
  
  dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNa7e581b5b6e98cff795e40261b8f5e75 sio:SIO_000628 miriam-gene:348, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_provenance {
  dgn-np:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_assertion dcterms:description
      "[We have characterized amyloid beta peptide (Abeta) concentration, Abeta deposition, paired helical filament formation, cerebrovascular amyloid angiopathy, apolipoprotein E (ApoE) allotype, and synaptophysin concentration in entorhinal cortex and superior frontal gyrus of normal elderly control (ND) patients, Alzheimer's disease (AD) patients, and high pathology control (HPC) patients who meet pathological criteria for AD but show no synapse loss or overt antemortem symptoms of dementia.]. 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:10487842;
    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:NP170757.RAXEuVQddXbcadq2ClNaoGczKUyOc2nruzeloldARVavc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}