@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q> .
@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:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_head {
  this: np:hasAssertion dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion;
    np:hasProvenance dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance;
    np:hasPublicationInfo dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion a np:Assertion .
  
  dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance a np:Provenance .
  
  dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion {
  miriam-gene:259197 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGNfe8a5ece70331f9bd66048734b41fb09 sio:SIO_000628 miriam-gene:259197, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance {
  dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_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-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:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:55+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" .
}