@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA> .
@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:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_head {
   this: np:hasAssertion dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion ;
    np:hasProvenance dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance ;
    np:hasPublicationInfo dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion a np:Assertion .
  dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance a np:Provenance .
  dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_assertion {
   miriam-gene:867 a ncit:C16612 .
  lld:C0023480 a ncit:C7057 .
  dgn-gda:DGNaa7408d8b711b4f9dfb3cf8b5f4f99b3 sio:SIO_000628 miriam-gene:867 , lld:C0023480 ;
    a sio:SIO_001121 .
}
dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_provenance {
   dgn-np:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_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:NP477305.RA0PqCFxOx-GYn03hZkQMsWaQUUvFi4PF4Xe2keMWWpMA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:46+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" .
}