@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4> .
@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:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_head {
  this: np:hasAssertion dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_assertion;
    np:hasProvenance dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_provenance;
    np:hasPublicationInfo dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_assertion a np:Assertion .
  
  dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_provenance a np:Provenance .
  
  dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_assertion {
  miriam-gene:259197 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNb6862ac2f6d3ab8ea47cb35b0aaa891c sio:SIO_000628 miriam-gene:259197, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_provenance {
  dgn-np:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_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:NP798098.RAxV7og4QIIiR694y8smIZRtJv2EDBebhAz8OOdBpXzR4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}