@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs> .
@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:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_head {
  this: np:hasAssertion dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_assertion;
    np:hasProvenance dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_provenance;
    np:hasPublicationInfo dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_provenance a np:Provenance .
  
  dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_assertion {
  miriam-gene:1999 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN44f31843c4290ce17b439abdf4af39d7 sio:SIO_000628 miriam-gene:1999, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_provenance {
  dgn-np:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_assertion dcterms:description
      "[We here show for the first time that the most common genomic copy number gains in breast cancer, 1q21 and 1q32, are associated with overexpression of the ETS transcription factors ETV3 and ELF3 (but not ELK4) at these loci irrespective of molecular subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP161108.RAtVLIiovOVVuCUQbtcowHAVYx7lwFacTdtVxYmesoOvs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}