@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_head {
  this: np:hasAssertion dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_assertion ;
    np:hasProvenance dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_provenance ;
    np:hasPublicationInfo dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_provenance a np:Provenance .
  dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_assertion {
  miriam-gene:3342 a ncit:C16612 .
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}
dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_provenance {
  dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_assertion dcterms:description "[In this review, we illustrate how the combination of three different microarray technologies, cDNA, CGH, and tissue microarrays, makes it possible to directly identify genes involved in chromosomal rearrangements in cell line model systems and then rapidly explore their significance as potential diagnostic and therapeutic targets in human primary breast cancer progression.]. 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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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP330534.RAxztp3i58wmEVmMH5s6YL_7lcm6A2dqcJWp4_nSxI750130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:15+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}