@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE> .
@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:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_head {
  this: np:hasAssertion dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion;
    np:hasProvenance dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance;
    np:hasPublicationInfo dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion a np:Assertion .
  
  dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance a np:Provenance .
  
  dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion {
  miriam-gene:9555 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN53a3b61e2ad610c584188bd874822f9f sio:SIO_000628 miriam-gene:9555, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_provenance {
  dgn-np:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_assertion dcterms:description
      "[These results show the power of combined array CGH and SAGE analysis for the identification of candidate amplicon targets and identify H2AFJ and EPS8 as novel putative oncogenes in breast cancer.]. 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:16618726;
    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:NP316912.RAVhfEV22H8meVQ50yxn_nEoPmfknu1bbv5VPbIZke-YE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}