@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o> .
@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 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:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_head {
  this: np:hasAssertion dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_assertion;
    np:hasProvenance dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_provenance;
    np:hasPublicationInfo dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_assertion a np:Assertion .
  
  dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_provenance a np:Provenance .
  
  dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_assertion {
  miriam-gene:1743 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN65bed8c074d90f460f849eb7f262b583 sio:SIO_000628 miriam-gene:1743, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_provenance {
  dgn-np:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_assertion dct:description
      "[We found no strong evidence of association for any of these loci with AD in this population. While the possibility exists that the genes analysed are involved in AD (ie they have weak effects and/or are population specific), results reinforce the need for extensive replication studies if we are to be successful in defining true risk factors in complex diseases.]. 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:11436125;
    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:NP45523.RAqx95An6jBdaLXu2xUTwCYJ6lN-k7GTc7sEUoXTBYN7o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}