@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY> .
@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:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_head {
   this: np:hasAssertion dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_assertion ;
    np:hasProvenance dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_provenance ;
    np:hasPublicationInfo dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_assertion a np:Assertion .
  dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_provenance a np:Provenance .
  dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_assertion {
   miriam-gene:2146 a ncit:C16612 .
  lld:C0023480 a ncit:C7057 .
  dgn-gda:DGN713ad7ede9fd1381b21c0b3f3edaa71b sio:SIO_000628 miriam-gene:2146 , lld:C0023480 ;
    a sio:SIO_001121 .
}
dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_provenance {
   dgn-np:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_assertion dcterms:description "[We genotyped ASXL1 and up to 18 other genes including epigenetic (TET2, EZH2, IDH1, IDH2, DNMT3A), splicing (SF3B1, SRSF2, ZRSF2, U2AF1), transcription (RUNX1, NPM1, TP53), and signaling (NRAS, KRAS, CBL, JAK2, FLT3) regulators in 312 patients with CMML.]. 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:23690417 ;
    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:NP488147.RAUDxDYUOWwnU3kramgA7fpEA0sG8shIvrUVLwl4HkNpY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:51+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 ;
    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" .
}