@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_head {
  this: np:hasAssertion dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion;
    np:hasProvenance dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance;
    np:hasPublicationInfo dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion a np:Assertion .
  
  dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance a np:Provenance .
  
  dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion {
  miriam-gene:5914 a ncit:C16612 .
  
  lld:C0023487 a ncit:C7057 .
  
  dgn-gda:DGN2519780e21bd7b66b7cb2b0874c00c3e sio:SIO_000628 miriam-gene:5914, lld:C0023487;
    a sio:SIO_001121 .
}

dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance {
  dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion dcterms:description
      "[Epigenetic alterations have been described in several AMLs, and in some cases their origin has been studied in detail mechanistically (such as in acute promyelocytic leukemia, caused by the promyelocytic leukemia-retinoic acid receptor-α fusion protein).]. 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:25369368;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:05+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}