@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48> .
@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:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_head {
  this: np:hasAssertion dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_assertion ;
    np:hasProvenance dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_provenance ;
    np:hasPublicationInfo dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_provenance a np:Provenance .
  dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_assertion {
  miriam-gene:10923 a ncit:C16612 .
  lld:C1961102 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_provenance {
  dgn-np:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_assertion dcterms:description "[We performed a comprehensive analysis of the deletion and the methylation profile of CDKN2A (hereafter identified separately as p16 and p14, for the different proteins encoded) and CDKN2B (hereafter p15) in 91 newly diagnosed B-ALL patients (61 children, 30 adults).]. 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:19837270 ;
    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:NP202260.RAKryTpYK4YnBGSAzjF76ZTN0uyGQ-_-3JOMPIRXRrK48130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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 ;
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}