@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo> .
@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:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_head {
  this: np:hasAssertion dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_assertion;
    np:hasProvenance dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_provenance;
    np:hasPublicationInfo dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_assertion a np:Assertion .
  
  dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_provenance a np:Provenance .
  
  dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN572a1509a075ca585d5006db0404d05f sio:SIO_000628 miriam-gene:348, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_provenance {
  dgn-np:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_assertion dcterms:description
      "[As the Apolipoprotein E (APOE) ɛ4 allele is a major genetic risk factor for sporadic Alzheimer's disease (AD), which has been suggested as a disconnection syndrome manifested by the disruption of white matter (WM) integrity and functional connectivity (FC), elucidating the subtle brain structural and functional network changes in cognitively normal ɛ4 carriers is essential for identifying sensitive neuroimaging based biomarkers and understanding the preclinical AD-related abnormality development.]. 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:25403724;
    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:NP1238037.RAqbiya8R4rmWJKgDota5XraXRAaArQdboA3XcdWBLRwo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:07+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" .
}