@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I> .
@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:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_head {
  this: np:hasAssertion dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_assertion;
    np:hasProvenance dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_provenance;
    np:hasPublicationInfo dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_assertion a np:Assertion .
  
  dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_provenance a np:Provenance .
  
  dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_assertion {
  miriam-gene:3417 a ncit:C16612 .
  
  lld:C0023480 a ncit:C7057 .
  
  dgn-gda:DGNc6a54ed0ea5bda2bb07b803f29b36f46 sio:SIO_000628 miriam-gene:3417, lld:C0023480;
    a sio:SIO_001121 .
}

dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_provenance {
  dgn-np:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_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:NP807849.RAixXCEdNVCBGDJuF4gAOvbI4N_kFKmtNOOqi78wrCn9I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}