@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g> .
@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:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_head {
  this: np:hasAssertion dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion;
    np:hasProvenance dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance;
    np:hasPublicationInfo dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion a np:Assertion .
  
  dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance a np:Provenance .
  
  dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C1270972 a ncit:C7057 .
  
  dgn-gda:DGN1e95f8f8e2103a510312a3d4a7aad0fa sio:SIO_000628 miriam-gene:348, lld:C1270972;
    a sio:SIO_001121 .
}

dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_provenance {
  dgn-np:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_assertion dcterms:description
      "[To determine whether memory loss is detectable before the symptomatic presentation of mild cognitive impairment (MCI) in those at greater genetic risk for Alzheimer disease (AD) based upon presence or absence of the e4 allele of APOE.]. 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:15184602;
    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:NP177798.RAcbhAJ_vCleib36F43x6zOwXOOCC8PbR5NTdkWJWL-2g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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>,
      <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" .
}