@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI> .
@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:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_head {
  this: np:hasAssertion dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion ;
    np:hasProvenance dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance ;
    np:hasPublicationInfo dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion a np:Assertion .
  dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance a np:Provenance .
  dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion {
  miriam-gene:10058 a ncit:C16612 .
  lld:C1333295 a ncit:C7057 .
  dgn-gda:DGN8df28ef80f0604a93df13512d5d98a22 sio:SIO_000628 miriam-gene:10058 , lld:C1333295 ;
    a sio:SIO_001121 .
}
dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_provenance {
  dgn-np:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_assertion dcterms:description "[A comparison of genome profiles of distinct subgroups of DLBCL demonstrated that (1) ABC DLBCL is characterized by gain of 3q, 18q, and 19q and loss of 6q and 9p21, and GCB DLBCL is characterized by gain of 1q, 2p, 7q, and 12q; (2) the genomic imbalances characteristic of the CD5(+) and CD5(-)CD10(+) groups were similar to those of the ABC and GCB types, respectively.]. 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:15886317 ;
    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:NP229956.RAVLYcQKiVeU29tgWLCRxRot3DIqTitQnvDff53IvLAoI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}