@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A> .
@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:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_head {
  this: np:hasAssertion dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_assertion;
    np:hasProvenance dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_provenance;
    np:hasPublicationInfo dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_assertion a np:Assertion .
  
  dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_provenance a np:Provenance .
  
  dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_assertion {
  miriam-gene:7153 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN1cb8a98871cb3ae04c1fa2281b3754fa sio:SIO_000628 miriam-gene:7153, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_provenance {
  dgn-np:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_assertion dcterms:description
      "[Amplification of at least one gene near ERBB2, topoisomerase IIalpha (TOP2A), has been shown to be clinically significant, but the prevailing patterns of gene amplification in this region of chromosome arm 17q have not been studied systematically in clinical cases of 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:15034864;
    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:NP290125.RAAEL08dYRrf9HybvrPF_yuplUCS-GlJ0quL6ZARXwB_A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}