@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928> .
@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/v4.0.0/void/> .

dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_head {
  this: np:hasAssertion dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_assertion;
    np:hasProvenance dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_provenance;
    np:hasPublicationInfo dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_assertion a np:Assertion .
  
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  dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0011269 a ncit:C7057 .
  
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dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_provenance {
  dgn-np:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_assertion dcterms:description
      "[We examined apolipoprotein E (Apo E) polymorphism and methylenetetrahydrofolate reductase (MTHFR) 677 C to T mutation by using the polymerase chain reaction (PCR) method in 100 elderly Japanese aged 60 or more, and assessed whether these genetic factors are associated with an increased risk for the clinical phenotypes of senile dementia, Alzheimer's disease (AD) and vascular dementia (VD) by cross-sectional survey.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-2016;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP286781.RAVYlnLgofXl3ahJvbG4ksAVWNSS8hKEcCLNeW4rnx928130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:55+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
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