@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k> .
@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:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_head {
  this: np:hasAssertion dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_assertion;
    np:hasProvenance dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_provenance;
    np:hasPublicationInfo dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_assertion a np:Assertion .
  
  dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_provenance a np:Provenance .
  
  dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0334634 a ncit:C7057 .
  
  dgn-gda:DGNa1aad2e53d2a62fc6a05842eec01759f sio:SIO_000628 miriam-gene:595, lld:C0334634;
    a sio:SIO_001121 .
}

dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_provenance {
  dgn-np:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_assertion dcterms:description
      "[Mantle cell lymphoma (MCL) is genetically characterized by 11q13 translocations leading to the overexpression of CCND1, and additional secondary genomic alterations that may be important in the progression of this disease.]. 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:18709664;
    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:NP169481.RAY3zYWZ7ZFIKQ3cC5iE03JodKcoEL2xCEZQOniDAsZ8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}