@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c> .
@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:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_head {
  this: np:hasAssertion dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion;
    np:hasProvenance dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance;
    np:hasPublicationInfo dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion a np:Assertion .
  
  dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance a np:Provenance .
  
  dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0038525 a ncit:C7057 .
  
  dgn-gda:DGN299a83f895beab47ffc8a57cd9b32f1e sio:SIO_000628 miriam-gene:348, lld:C0038525;
    a sio:SIO_001122 .
}

dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_provenance {
  dgn-np:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_assertion dcterms:description
      "[Presence of the APOE4 allele is associated with poorer response to traumatic brain injury and ischemic stroke, but the association between APOE genotype and outcome following aneurysmal subarachnoid hemorrhage (SAH) remains unclear.]. 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:19017669;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48232.RAAukoadWTauU6BDIwdX99p0WvNG8dro26wDLDon4eU7c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}