@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0> .
@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:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_head {
  this: np:hasAssertion dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_assertion ;
    np:hasProvenance dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_provenance ;
    np:hasPublicationInfo dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_assertion a np:Assertion .
  dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_provenance a np:Provenance .
  dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  lld:C0019562 a ncit:C7057 .
  dgn-gda:DGN65d15fa2121e2a65da8fe6aa946e4432 sio:SIO_000628 miriam-gene:3342 , lld:C0019562 ;
    a sio:SIO_001121 .
}
dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_provenance {
  dgn-np:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_assertion dcterms:description "[In contrast to the near-diploidy of the low-grade lesions, a high-grade lesion and its nodal metastasis were markedly aneuploid, revealed loss of VHL by fluorescence in situ hybridization (FISH), and contained recurrent unbalanced translocations and losses of chromosome arms 2q, 3p, 4q, 9p, 14q, and 19p as demonstrated by comparative genomic hybridization (CGH).]. 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:11284029 ;
    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:NP402810.RAvDhEfqLVlYsVBtDLUzr7d_ftFJlSK8F2Rf7WJwA16h0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}