@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ> .
@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:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_head {
   this: np:hasAssertion dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_assertion ;
    np:hasProvenance dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_assertion a np:Assertion .
  dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_provenance a np:Provenance .
  dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_assertion {
   miriam-gene:1029 a ncit:C16612 .
  lld:C0025164 a ncit:C7057 .
  dgn-gda:DGNea566e0fb8ad2678440dd07e6f0d1a32 sio:SIO_000628 miriam-gene:1029 , lld:C0025164 ;
    a sio:SIO_001121 .
}
dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_provenance {
   dgn-np:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_assertion dcterms:description "[Mean copy number of CDKN2A and CEP9 and frequency of nuclei with loss of PIK3CA were significantly different in the CM group compared with normal mucosa and marginal levels of deletions in TP63, FHIT, PIK3CA, EGFR, CDKN2A, YES and gains at PIK3CA, TP63, FGFR1, MYC, CDNK2A and NCOA3 were detected in few CM cases, mainly with dilation grades III and IV.]. 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:20163722 ;
    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:NP462812.RA0qZe6CQCWCfbhwmNld0vy5UNS_mvOGBLF4i9dBTJqnQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:35+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" .
}