@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM> .
@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:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_head {
  this: np:hasAssertion dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion;
    np:hasProvenance dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance;
    np:hasPublicationInfo dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion a np:Assertion .
  
  dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance a np:Provenance .
  
  dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGNd76b00df2d1a154de4de50dd9a193801 sio:SIO_000628 miriam-gene:348, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_provenance {
  dgn-np:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_assertion dcterms:description
      "[Results confirmed that APOE 4 allele associated with increased NFT stages and cognitive decline, with carriers with one APOE ε2 or ε3 allele often having better clinical outcomes compared to carriers with none or two ε2 or ε3 alleles respectively.]. 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:21605063;
    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:NP896156.RANhuMCWvnSdEEi1MeUZH20ZvQIdo5vuJlSGG_K7D8NJM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:30+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" .
}