@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w> .
@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:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_head {
  this: np:hasAssertion dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_assertion ;
    np:hasProvenance dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_provenance ;
    np:hasPublicationInfo dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_assertion a np:Assertion .
  dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_provenance a np:Provenance .
  dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_assertion {
  miriam-gene:5914 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_provenance {
  dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_assertion dcterms:description "[Additional FISH studies that use probes to the SMS, RARA, and TP53 genes are an effective way to determine the true HER2 amplification status in patients with polysomy 17 and they have important potential implications for guiding HER2-targeted therapy 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:21947821 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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}
dgn-np:NP477290.RAqU3R-yyzGS1Wgrzv4g4KofZ9J5IX44z1dNfszVWzy9w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:46+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}