@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A> .
@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:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_head {
  this: np:hasAssertion dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_assertion ;
    np:hasProvenance dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_provenance ;
    np:hasPublicationInfo dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_assertion a np:Assertion .
  dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_provenance a np:Provenance .
  dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0001418 a ncit:C7057 .
  dgn-gda:DGN296eec61fcd2d5c146625813d05a8693 sio:SIO_000628 miriam-gene:1956 , lld:C0001418 ;
    a sio:SIO_001121 .
}
dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_provenance {
  dgn-np:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_assertion dcterms:description "[In addition to the clinical benefit, understanding EGFR mutations sheds new light on the molecular and pathological aspects of this adenocarcinoma subset, which include frequent development in nonsmokers or females, and particular clusters within the molecular classification in lung cancer.]. 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:20135199 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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:NP792111.RAq4EbrVAozPQSa8DYANsl3mDuYcwRGkUNvvee3_Tsw_A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:44+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}