@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo> .
@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:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_head {
  this: np:hasAssertion dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_assertion ;
    np:hasProvenance dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_provenance ;
    np:hasPublicationInfo dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_assertion a np:Assertion .
  dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_provenance a np:Provenance .
  dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_assertion {
  miriam-gene:84106 a ncit:C16612 .
  lld:C0242596 a ncit:C7057 .
  dgn-gda:DGN6d9241751d5523ef515f45a029428407 sio:SIO_000628 miriam-gene:84106 , lld:C0242596 ;
    a sio:SIO_001121 .
}
dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_provenance {
  dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_assertion dcterms:description "[These results indicate that qrtPCR monitoring of PML-RAR alpha NQ can identify patients at high risk of relapse and suggest that clinically practical PB NQ monitoring at more frequent FUP intervals may improve predictive accuracy for relapse or continuing CR in patients with persistent, fluctuating minimal residual disease levels.]. 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:12468436 ;
    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 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP691793.RAjVTbeLnKQraNfRqS6cnpvFVOngTdNZ9avppFi6WqhOo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}