@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ> .
@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:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_head {
  this: np:hasAssertion dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion;
    np:hasProvenance dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance;
    np:hasPublicationInfo dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion a np:Assertion .
  
  dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance a np:Provenance .
  
  dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion {
  miriam-gene:6520 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN79a821215daf92d98cbbf93e7721c5c1 sio:SIO_000628 miriam-gene:6520, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_provenance {
  dgn-np:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_assertion dcterms:description
      "[It is worthwhile to point out that such a highly polymorphic DNA sequence is located in the same chromosomal region where so much somatic rearrangement goes on normally (i.e., switch region between classes of heavy chain constant region genes) and which is involved with de novo translocations associated with malignancies.]. 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:6818543;
    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:NP196014.RAYaeHx0A6Vr6kLP7zgqvGw_TUSwGBxQMWH21VvW_y5QQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}