@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU> .
@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:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_head {
  this: np:hasAssertion dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_assertion ;
    np:hasProvenance dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_provenance ;
    np:hasPublicationInfo dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_assertion a np:Assertion .
  dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_provenance a np:Provenance .
  dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  lld:C0010606 a ncit:C7057 .
  dgn-gda:DGN494a5ada7512b22044da6564b6e4d402 sio:SIO_000628 miriam-gene:5728 , lld:C0010606 ;
    a sio:SIO_001121 .
}
dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_provenance {
  dgn-np:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_assertion dcterms:description "[The aim of the present study was to analyse two high grade transformation adenoid cystic carcinomas (hgACC) and one hybrid tumour in order to identify, by mutational and microsatellite analysis, genetic alterations in TP53, CDKN2A/ARF, RAS, BRAF, PTEN, MAPK2 and EGFR genes.]. 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:21503581 ;
    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:NP181885.RAVn2FqojfZBFVvKX3cxG6BCaX-qmLtXsnyPpWu-uEuvU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}