@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ> .
@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:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_head {
  this: np:hasAssertion dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_assertion;
    np:hasProvenance dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_assertion a np:Assertion .
  
  dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_provenance a np:Provenance .
  
  dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_assertion {
  miriam-gene:2309 a ncit:C16612 .
  
  lld:C1947901 a ncit:C7057 .
  
  dgn-gda:DGN3f03378762884fe741eda20b5e56d983 sio:SIO_000628 miriam-gene:2309, lld:C1947901;
    a sio:SIO_001121 .
}

dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_provenance {
  dgn-np:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_assertion dcterms:description
      "[As such, sustained nuclear FOXO3a expression in breast cancer may culminate in cancer progression and the development of an aggressive phenotype similar to that observed in cytotoxic chemotherapy resistant breast cancer cell models.]. 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:20808831;
    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:NP793689.RAPrN9jD7SBCrg82t5bbV5TTMDLFfwtW6CCJoEcoh1lGQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:07+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" .
}