@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A> .
@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:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_head {
  this: np:hasAssertion dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_assertion;
    np:hasProvenance dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_provenance;
    np:hasPublicationInfo dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_assertion a np:Assertion .
  
  dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_provenance a np:Provenance .
  
  dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGNc2336eff9edf83bfaa8623b2b55fdab4 sio:SIO_000628 miriam-gene:7157, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_provenance {
  dgn-np:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_assertion dcterms:description
      "[Genomic features including unmutated immunoglobulin variable region heavy chain (IgVH) genes, del(11q22.3), del(17p13.1), and p53 mutations have been reported to predict the clinical course and overall survival of patients with chronic lymphocytic leukemia (CLL).]. 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:17283363;
    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:NP592552.RA0ESxJ63IEGPaOjp4gFENQWPF9_LG2-Z-23n-7sCcR7A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:14+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" .
}