@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA> .
@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:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_head {
  this: np:hasAssertion dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_assertion;
    np:hasProvenance dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_provenance;
    np:hasPublicationInfo dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_assertion a np:Assertion .
  
  dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_provenance a np:Provenance .
  
  dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_assertion {
  miriam-gene:4869 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN60c874dc713359e5bf5efcb34745088c sio:SIO_000628 miriam-gene:4869, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_provenance {
  dgn-np:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_assertion dcterms:description
      "[To explore the validity and prognostic significance of minimal residual disease detection by quantitative polymerase chain reaction (qPCR) in patients of acute myeloid leukemia (AML) bearing Nucleophosmin (NPM1) mutations, we quantified mutants in 194 bone marrow samples from 38 patients with a median follow-up time of 20.6 months.]. 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:17361227;
    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:NP599112.RAPIxOPXNUrP_1gI4wovgK8QWadKRWshkccvB98nXN3MA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:17+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}