@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs> .
@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:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_head {
  this: np:hasAssertion dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_assertion ;
    np:hasProvenance dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_provenance ;
    np:hasPublicationInfo dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_assertion a np:Assertion .
  dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_provenance a np:Provenance .
  dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_assertion {
  miriam-gene:171023 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_provenance {
  dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_assertion dcterms:description "[The present study was designed to establish the incidence of cytogenetic evolution (CE), defined as the acquisition of chromosomal defects during the course of MDS, in order to correlate it with the WHO classification and IPSS score, and to assess its impact on overall survival (OS) and risk of MDS/AML evolution (progression-free interval, PFI) by means of Cox models for time-dependent covariates.]. 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-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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 ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP798967.RAZe9i3JUoKS9jjYSWV9026XWrr3bYHraSAS78uUsJWHs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:47+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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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}