@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4> .
@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:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_head {
  this: np:hasAssertion dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion ;
    np:hasProvenance dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance ;
    np:hasPublicationInfo dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance a np:Provenance .
  dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion {
  miriam-gene:3342 a ncit:C16612 .
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dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance {
  dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion dcterms:description "[This study indicates that the frequency of genetic alterations in PC as detected by CGH correlates with clinical outcome, and that losses of DNA from chromosomes 6q and 13q are important events that correlate with tumor progression, with loss of 13q, especially instability of locus 171, also associated with angiogenesis.]. 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 ;
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}
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}