@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc> .
@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:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_head {
  this: np:hasAssertion dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_assertion ;
    np:hasProvenance dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_provenance ;
    np:hasPublicationInfo dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_assertion a np:Assertion .
  dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_provenance a np:Provenance .
  dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0040100 a ncit:C7057 .
  dgn-gda:DGNe453928b217781a2c5af6db507b5f2d4 sio:SIO_000628 miriam-gene:1956 , lld:C0040100 ;
    a sio:SIO_001121 .
}
dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_provenance {
  dgn-np:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_assertion dcterms:description "[We have investigated 20 different subtypes of thymomas (type A, AB, and B3) and thymic carcinomas for mutations in exons 18, 19, 20, and 21 of the EGFR gene and performed immunohistochemistry for 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:16919868 ;
    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:NP652007.RAnEMxODTE5dgreMaUPulni0V4r0wNEbgEXRNrgUf3amc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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> ;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}