@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI> .
@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:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_head {
  this: np:hasAssertion dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_assertion;
    np:hasProvenance dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_provenance;
    np:hasPublicationInfo dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_assertion a np:Assertion .
  
  dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_provenance a np:Provenance .
  
  dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_assertion {
  miriam-gene:4888 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_provenance {
  dgn-np:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_assertion dcterms:description
      "[The effects of haplotypes for 2 PP2A regulatory subunit genes, PP2 regulatory subunit B alpha isoform (PPP2R2A) and PP2A regulatory subunit B' epsilon isoform (PPP2R5E) on breast cancer risk were nominally significant but did not remain significant after the analysis was adjusted for multiple comparisons.]. 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:19890961;
    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:NP934799.RA714eHfRljxsfWe_HRE6eaBG3F1-dMMzKLh8GGJ2lBEI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:33+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}