@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4> .
@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:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_head {
  this: np:hasAssertion dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion ;
    np:hasProvenance dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance a np:Provenance .
  dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion {
  miriam-gene:1027 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_provenance {
  dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_assertion dcterms:description "[Those results suggest that (a) overexpression of Skp2 through an amplification mechanism may contribute to the progression of BTC, (b) not only each molecule, but also the combination of Skp2 and p27Kip1, might be a useful predictor of the prognosis of BTC, and (c) molecular targets of Skp2 other than p27Kip1 may also be important factors in the pathogenesis of this disease.]. 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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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP615610.RAUvgxvnqL1ipbOT5ReNUbZ8iDjZFc9gzCfPOR5-HxyW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:12+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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