@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI> .
@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:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_head {
  this: np:hasAssertion dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_assertion;
    np:hasProvenance dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_provenance;
    np:hasPublicationInfo dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_assertion a np:Assertion .
  
  dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_provenance a np:Provenance .
  
  dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_assertion {
  miriam-gene:5290 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNd329c5e78c935200753efe263b902f8d sio:SIO_000628 miriam-gene:5290, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_provenance {
  dgn-np:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_assertion dcterms:description
      "[While the PI3K/Akt pathway has been shown to regulate multiple cellular events pertinent to AD pathogenesis, potential functions of tumor suppressor phosphatase and tensin homologue deleted on chromosome 10 (PTEN) in AD pathogenesis have not been 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:16645045;
    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:NP884041.RAlzISjTwJTm1wxhFEBE7PoPpCrGSJ5Ewj1mYkdBOVOVI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}