@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0> .
@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:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_head {
  this: np:hasAssertion dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_assertion;
    np:hasProvenance dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_provenance;
    np:hasPublicationInfo dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_assertion a np:Assertion .
  
  dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_provenance a np:Provenance .
  
  dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_assertion {
  miriam-gene:5027 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN06ec85c43abe0fbc78af15c987c2cafa sio:SIO_000628 miriam-gene:5027, lld:C0023418;
    a sio:SIO_001122 .
}

dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_provenance {
  dgn-np:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_assertion dcterms:description
      "[The P2X7 polymorphism could affect clinical outcome in CLL, especially in patients with mutated V(H) genes. Studies are necessary to elucidate the biological role of the P2X7 polymorphism in CLL in vivo.]. 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:12493261;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP66921.RAebZQ_AS1fuygd5X1OvLcWkFfgBJkaQecpuGDZ1sCrI0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:16+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}