@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU> .
@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 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:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_head {
   this: np:hasAssertion dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_assertion ;
    np:hasProvenance dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_provenance ;
    np:hasPublicationInfo dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_assertion a np:Assertion .
  dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_provenance a np:Provenance .
  dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_assertion {
   miriam-gene:51750 a ncit:C16612 .
  lld:C0024305 a ncit:C7057 .
  dgn-gda:DGNa226efeaf66f873c3f854055a2a5b31c sio:SIO_000628 miriam-gene:51750 , lld:C0024305 ;
    a sio:SIO_001121 .
}
dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_provenance {
   dgn-np:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_assertion dct:description "[In order to improve the cytomorphologic diagnosis of malignant lymphoma on lymph node fine-needle aspiration (FNA), and to make a confident discrimination between low-grade follicular non-Hodgkin's lymphoma (NHL) and lymphoid hyperplasia, polymerase chain reaction (PCR) analysis was performed of the Ig CDR3 region and BCL2 breakpoint region in 25 nonselected cases of malignant lymphoma (17 NHL and 8 Hodgkin's disease [HD]) with histologic control, and 22 cases of lymph nodal hyperplasia with histologic and/or clinical control.]. 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:9276187 ;
    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:NP360903.RAD_RUKeOo1QZI_hChp5qzewpR7MtvDwylR_SCnTa9vYU130_publicationInfo {
   this: dct:created "2014-10-02T12:35:31+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}