@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c> .
@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:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_head {
  this: np:hasAssertion dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_assertion;
    np:hasProvenance dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_provenance;
    np:hasPublicationInfo dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_assertion a np:Assertion .
  
  dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_provenance a np:Provenance .
  
  dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_assertion {
  miriam-gene:2555 a ncit:C16612 .
  
  lld:C0001973 a ncit:C7057 .
  
  dgn-gda:DGN06cd0831f10bf4fac688dccc4c139d78 sio:SIO_000628 miriam-gene:2555, lld:C0001973;
    a sio:SIO_001122 .
}

dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_provenance {
  dgn-np:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_assertion dcterms:description
      "[These findings suggest that genetic variants of GABRA2 increase risk for AD in the Russian population and provide additional support to the hypothesis that polymorphic variation at the GABRA2 locus plays an important role in predisposing to AD at least in European-ancestry populations.]. 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:15834213;
    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:NP43778.RAQED_BDwACrMB8xW8LJIhuCmRofnXSQlpc6ajrSO379c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}