@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA> .
@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:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_head {
  this: np:hasAssertion dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion;
    np:hasProvenance dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance;
    np:hasPublicationInfo dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion a np:Assertion .
  
  dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance a np:Provenance .
  
  dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion {
  miriam-gene:611 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGN7dea29036b67b7878335313f674133b9 sio:SIO_000628 miriam-gene:611, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_provenance {
  dgn-np:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_assertion dcterms:description
      "[In this study on 27 t(4;11) infant ALL, we have used standardized primer sets for the detection of all incomplete and complete immunoglobulin (Ig) heavy chain (IGH) rearrangements, as well as for the Ig light chain kappa (IGK), T-cell receptor delta (TCRD) and gamma (TCRG) rearrangements that are most common in childhood BCP ALL.]. 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:11972513;
    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:NP188652.RA2zzpkhtiGS-p70xXEyF8iVp0WN7xdXI9yoZcWuL7vgA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}