@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA> .
@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:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_head {
  this: np:hasAssertion dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion;
    np:hasProvenance dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance;
    np:hasPublicationInfo dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion a np:Assertion .
  
  dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance a np:Provenance .
  
  dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion {
  miriam-gene:5290 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN202b60a1833570efae3c4a555de9cd23 sio:SIO_000628 miriam-gene:5290, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_provenance {
  dgn-np:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_assertion dcterms:description
      "[The phosphoinositide 3-kinase (PI3K)/Akt pathway has been implicated in the pathogenesis of AD, however, potential functions and role of tumor suppressor phosphatase and tensin homologue deleted on chromosome 10 (PTEN) in AD pathogenesis have not been fully explored.]. 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:22906543;
    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:NP881744.RAfA0ZIXVB1s3RJMqY4SAMEyOVFSlbWHSuF6G_550L5lA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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" .
}