@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE> .
@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:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_head {
  this: np:hasAssertion dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion;
    np:hasProvenance dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance;
    np:hasPublicationInfo dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion a np:Assertion .
  
  dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance a np:Provenance .
  
  dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion {
  miriam-gene:2146 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNb807eca378dd0bb29898dbaa8a5a15e3 sio:SIO_000628 miriam-gene:2146, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_provenance {
  dgn-np:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_assertion dcterms:description
      "[Recent extensive mutation analyses of the myeloid malignancies have revealed that inactivating somatic mutations in PcG genes such as EZH2 and ASXL1 occur frequently in patients with myelodysplastic disorders including myelodysplastic syndromes (MDSs) and MDS/myeloproliferative neoplasm (MPN) overlap disorders (MDS/MPN).]. 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:24218139;
    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:NP186670.RABiNmZyEKBiY2mXQBHNEYz9wV656qmoKnk2u7rFrTemE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}