@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30> .
@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:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_head {
  this: np:hasAssertion dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion ;
    np:hasProvenance dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance ;
    np:hasPublicationInfo dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion a np:Assertion .
  dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance a np:Provenance .
  dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  lld:C0242596 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_provenance {
  dgn-np:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_assertion dcterms:description "[This is because the issue of the benefits of achieving MRD-negative status in patients with CLL requires further investigation in large controlled trials, in which patients should be stratified according to not only clinical variables but also biological parameters such as cytogenetics, IGHV mutations or ZAP-70 expression.]. 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:20620974 ;
    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:NP411817.RA15q50PKDbD7mlCYXY4gwNAxmK8zaK14wS09_kyCAq30130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:04+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" .
}