@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U> .
@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:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_head {
  this: np:hasAssertion dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion ;
    np:hasProvenance dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance ;
    np:hasPublicationInfo dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion a np:Assertion .
  dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance a np:Provenance .
  dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion {
  miriam-gene:3417 a ncit:C16612 .
  lld:C1458156 a ncit:C7057 .
  dgn-gda:DGN4d63b891ba9182f623e627ae66974a36 sio:SIO_000628 miriam-gene:3417 , lld:C1458156 ;
    a sio:SIO_001121 .
}
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance {
  dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion dcterms:description "[We investigated the IDH1 gene mutation status by nested PCR and denaturing gradient gel electrophoresis (DGGE) on DNA extracted from archival tumor blocks of 63 glioma patients who were treated following recurrence with the epidermal growth factor receptor (EGFR)-targeted blocking monoclonal antibody cetuximab, or the vascular endothelial growth factor (receptor) (VEGF(R))-targeted agents sunitinib malate and bevacizumab.]. 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:22199315 ;
    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:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:43+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" .
}