@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0> .
@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:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_head {
  this: np:hasAssertion dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_assertion;
    np:hasProvenance dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_provenance;
    np:hasPublicationInfo dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_assertion a np:Assertion .
  
  dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_provenance a np:Provenance .
  
  dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_assertion {
  miriam-gene:3934 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN65fcd8f8f9b221cef52608f3e6e7df59 sio:SIO_000628 miriam-gene:3934, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_provenance {
  dgn-np:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_assertion dcterms:description
      "[These results indicate a novel role for p25 in the secretory pathway and suggest that elevated levels of p25 and BACE1 in AD brains may contribute to altered neurotransmitter pathology of AD through enhancing spontaneous basal secretion.]. 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:20033852;
    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:NP580355.RAivie2wZylZuTrrIIAuJdFXeHf_GLsn2nUcoAQJjOQT0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:49+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}