@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4> .
@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:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_head {
  this: np:hasAssertion dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_assertion;
    np:hasProvenance dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_provenance;
    np:hasPublicationInfo dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_assertion a np:Assertion .
  
  dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_provenance a np:Provenance .
  
  dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_assertion {
  miriam-gene:351 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGNefa9beaf947fcb8cab22d6bc014d7cc8 sio:SIO_000628 miriam-gene:351, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_provenance {
  dgn-np:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_assertion dcterms:description
      "[In Alzheimer's disease (AD), endosome abnormalities are among the earliest neuropathologic features to develop and have now been closely linked to genetic risk factors for AD, including APP triplication in Trisomy 21 (Down syndrome, DS) and ApoE4 genotype in sporadic AD.]. 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:15639316;
    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:NP475383.RAXyqheiBnh8OGWxYWTNIKgz1RQBbdfJ3bnCTyuE6VFS4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:20+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" .
}