@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM> .
@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:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_head {
  this: np:hasAssertion dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion ;
    np:hasProvenance dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance ;
    np:hasPublicationInfo dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion a np:Assertion .
  dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance a np:Provenance .
  dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion {
  miriam-gene:4771 a ncit:C16612 .
  lld:C0027859 a ncit:C7057 .
  dgn-gda:DGNbc644034a7b57fa4103f1c756c2257d5 sio:SIO_000628 miriam-gene:4771 , lld:C0027859 ;
    a sio:SIO_001121 .
}
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance {
  dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion dcterms:description "[Importantly, high level amplifications have been observed on 16p and 16q as well as on 9q, suggesting the possible involvement of several oncogenes in the tumorigenesis of VS. Our data suggest the involvement of various oncogenes and tumor suppressor genes might play a role in the genesis of the vestibular schwannomas apart from the inactivation of the NF2 gene.]. 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:20872275 ;
    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:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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" .
}