@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA> .
@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/v3.0.0/void/> .

dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_head {
  this: np:hasAssertion dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_assertion;
    np:hasProvenance dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_provenance;
    np:hasPublicationInfo dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_assertion a np:Assertion .
  
  dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_provenance a np:Provenance .
  
  dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0003537 a ncit:C7057 .
  
  dgn-gda:DGN17652c4f0d1f000d8af161faec9b8214 sio:SIO_000628 miriam-gene:348, lld:C0003537;
    a sio:SIO_001121 .
}

dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_provenance {
  dgn-np:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_assertion dcterms:description
      "[On admission, there was no significant difference in the FIM or NIHSS measurements between the apo E4 group and other patients, but the prevalence of aphasia was 2.07 times more frequent in those with the APOE*E4 genotype (95% confidence interval, 0.98-4.4).]. 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:12881819;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP244802.RA4bycleDeVY9CuDiC2VGH-DMqmf4XTPfJt-G4JxjtpsA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:59+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}