@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg> .
@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:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_head {
  this: np:hasAssertion dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_assertion;
    np:hasProvenance dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_provenance;
    np:hasPublicationInfo dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_assertion a np:Assertion .
  
  dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_provenance a np:Provenance .
  
  dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_assertion {
  miriam-gene:596 a ncit:C16612 .
  
  lld:C0475801 a ncit:C7057 .
  
  dgn-gda:DGN11e012a7c69f79e3f16333e5fd46d357 sio:SIO_000628 miriam-gene:596, lld:C0475801;
    a sio:SIO_001121 .
}

dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_provenance {
  dgn-np:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_assertion dcterms:description
      "[Therefore, we examined 170 cases of B-cell chronic lymphocytic leukemia (B-CLL), 7 cases of B-cell prolymphocytic leukemia (B-PLL), 25 cases of hairy cell leukemia (HCL) and 22 cases of splenic lymphoma with villous lymphocytes (SLVL) with defined cytogenetic abnormalities by DNA blot using both 5' and 3' BCL2 probes to search for rearrangement of the BCL2 locus.]. 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:8204892;
    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:NP663126.RAIUYFTB260BUlsm552xK-1zJ9irc_EPcOK0k5U1xdzbg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}