@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_head {
  this: np:hasAssertion dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_assertion ;
    np:hasProvenance dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_provenance ;
    np:hasPublicationInfo dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_assertion a np:Assertion .
  dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_provenance a np:Provenance .
  dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_assertion {
  miriam-gene:673 a ncit:C16612 .
  lld:C0596263 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_provenance {
  dgn-np:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_assertion dcterms:description "[Here, we use massively parallel exome and targeted level sequencing of 132 sporadic cSCCs and of 39 squamoproliferative lesions and cSCCs arising in patients receiving the BRAF inhibitor vemurafenib, as well as 10 normal skin samples, to identify NOTCH1 mutation as an early event in squamous cell carcinogenesis.]. 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:24662767 ;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1166842.RAnk7dGC9NcWDh0FxZQA4RZE8lXVyzS58ttNdJb_a8WU4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:35+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}