@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ> .
@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/v3.0.0/void/> .

dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_head {
  this: np:hasAssertion dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_assertion;
    np:hasProvenance dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_provenance;
    np:hasPublicationInfo dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_assertion a np:Assertion .
  
  dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_provenance a np:Provenance .
  
  dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_assertion {
  miriam-gene:9437 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN4c2eff873755cfdcac8a6d34823d5fc1 sio:SIO_000628 miriam-gene:9437, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_provenance {
  dgn-np:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_assertion dcterms:description
      "[Our longitudinal study of AML patients showed that the NCR(dull) phenotype was acquired during leukemia development because we observed its complete (for NKp46) or partial (for NKp30) reversibility in patients achieving complete remission (CR).]. 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:16940427;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP823757.RAPJEruK3Y8bTMO_mLasLfWJdiGfSyfo6xCi1ILGeDNqQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:59+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}