@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8> .
@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:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_head {
  this: np:hasAssertion dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_assertion;
    np:hasProvenance dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_provenance;
    np:hasPublicationInfo dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_assertion a np:Assertion .
  
  dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_provenance a np:Provenance .
  
  dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_assertion {
  miriam-gene:3492 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGN5f4462669219027942ca2db276aaecf6 sio:SIO_000628 miriam-gene:3492, lld:C0023434;
    a sio:SIO_001122 .
}

dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_provenance {
  dgn-np:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_assertion dcterms:description
      "[In order to further investigate the T393C SNP in CLL, we have genotyped 279 CLL cases and correlated the genotypes to clinical outcome and other known prognostic factors such as the immunoglobulin heavy chain variable (IGHV) gene mutation status and CD38 expression.]. 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:18006055;
    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:NP640481.RALfsTpW4Qp-2qOL70WSNmtlkFk9-XOiMqN2-PNbWifI8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:35+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" .
}