@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA> .
@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 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:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_head {
  this: np:hasAssertion dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_assertion;
    np:hasProvenance dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_provenance;
    np:hasPublicationInfo dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_assertion a np:Assertion .
  
  dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_provenance a np:Provenance .
  
  dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_assertion {
  miriam-gene:10153 a ncit:C16612 .
  
  lld:C0011265 a ncit:C7057 .
  
  dgn-gda:DGNded7bc31966c2ba489631ff684522992 sio:SIO_000628 miriam-gene:10153, lld:C0011265;
    a sio:SIO_001121 .
}

dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_provenance {
  dgn-np:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_assertion dc:description
      "[Endocytic system dysfunction is one of the earliest disturbances that occur in Alzheimer's disease (AD), and may underlie the selective vulnerability of cholinergic basal forebrain (CBF) neurons during the progression 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:21669283;
    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:NP381391.RADYYWfteJNnATKIwwv-q_LeQO2myUh26CHhtR7vyI7MA130_publicationInfo {
  this: dc:created "2014-10-02T12:35:45+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}