@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU> .
@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:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_head {
  this: np:hasAssertion dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_assertion ;
    np:hasProvenance dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_provenance ;
    np:hasPublicationInfo dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_assertion a np:Assertion .
  dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_provenance a np:Provenance .
  dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_assertion {
  miriam-gene:6657 a ncit:C16612 .
  lld:C1168401 a ncit:C7057 .
  dgn-gda:DGN6a40ae25c98ec83aef5980ef524d5c3d sio:SIO_000628 miriam-gene:6657 , lld:C1168401 ;
    a sio:SIO_001121 .
}
dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_provenance {
  dgn-np:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_assertion dcterms:description "[Using an integrated genomic analysis and validation methodology we confirm four molecular classes of HNSCC (basal, mesenchymal, atypical, and classical) consistent with signatures established for squamous carcinoma of the lung, including deregulation of the KEAP1/NFE2L2 oxidative stress pathway, differential utilization of the lineage markers SOX2 and TP63, and preference for the oncogenes PIK3CA and EGFR.]. 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:23451093 ;
    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:NP267783.RAPY0KVmLdQ7MKhszKFt-mmmSCHTqrLRh8h1Higsdn9TU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}