@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I> .
@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:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_head {
  this: np:hasAssertion dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_assertion;
    np:hasProvenance dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_provenance;
    np:hasPublicationInfo dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_assertion a np:Assertion .
  
  dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_provenance a np:Provenance .
  
  dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_assertion {
  miriam-gene:4609 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGNbcf2021a8c8b3b546bb7e8d62e90aeca sio:SIO_000628 miriam-gene:4609, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_provenance {
  dgn-np:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_assertion dcterms:description
      "[The rarity of t(8;14) in CLL together with a cryptic deletion that probably includes the MYC gene in our CLL patient persuaded us to explore the clinicopathological role of MYC translocations by comparing disease progression in our patient and in other reported CLL cases.]. 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:16616107;
    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:NP545026.RA4ZbgZQg_GhGOfxPBmD6Vo0YxDfM4_yY6LegBE7dsz5I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:52+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" .
}