@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o> .
@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:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_head {
   this: np:hasAssertion dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_assertion ;
    np:hasProvenance dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_provenance ;
    np:hasPublicationInfo dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_assertion a np:Assertion .
  dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_provenance a np:Provenance .
  dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_assertion {
   miriam-gene:3342 a ncit:C16612 .
  lld:C0024301 a ncit:C7057 .
  dgn-gda:DGN269ece1ec6d9daddf3b79f9b60603b5a sio:SIO_000628 miriam-gene:3342 , lld:C0024301 ;
    a sio:SIO_001121 .
}
dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_provenance {
   dgn-np:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_assertion dcterms:description "[To determine the type and pattern of genomic instability occurring in histological transformation of FCLs and the role of DNA mismatch repair defects in this procedure, we have performed microsatellite analysis, comparative genomic hybridization (CGH) and mutational analysis of hMLH1 and hMSH2 genes on serial biopsy specimens from patients with FCL transformed to diffuse large cell lymphoma (DLCL).]. 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:11187904 ;
    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:NP549468.RAw9TIJ_znU_W6rQbe8TADifjlHy7q0LQ03aFCd3R0J5o130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:31+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> ;
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}