@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg> .
@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:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_head {
  this: np:hasAssertion dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion;
    np:hasProvenance dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance;
    np:hasPublicationInfo dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion a np:Assertion .
  
  dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance a np:Provenance .
  
  dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN0bc6dac537712000923a45bdeeb95848 sio:SIO_000628 miriam-gene:348, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_provenance {
  dgn-np:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_assertion dcterms:description
      "[We studied the allelic frequencies of ApoE in 26 DS cases fulfilling clinical diagnostic criteria for AD and in 26 DS controls matched for age, sex, and premorbid level of mental retardation.]. 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:7654070;
    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:NP740503.RAfxBdigm8VJrF96mdYT7OI5xao4v9maJBeG5K3LzUONg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}