@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc> .
@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:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_head {
  this: np:hasAssertion dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_assertion ;
    np:hasProvenance dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_provenance ;
    np:hasPublicationInfo dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_provenance a np:Provenance .
  dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_provenance {
  dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_assertion dcterms:description "[The relationship between APOE genotype (*E3/*E3, *E3/*E4, *E2/*E3, *E4/*E4, *E2/*E4, and *E2/*E2) and fatal and nonfatal CHD was examined among 10 035 men and 12 134 women, aged 440 to 79 years, from the Norfolk, England, arm of the European Prospective Into Nutrition and Cancer Study (1993-2007).]. 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:19667307 ;
    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 ;
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dgn-np:NP208826.RASzjEEAnA2j7dGGVmjOEnHoL6ZlsQmOTMuZNIfhQP9wc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:55+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 ;
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}