@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk> .
@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:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_head {
  this: np:hasAssertion dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion ;
    np:hasProvenance dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance ;
    np:hasPublicationInfo dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion a np:Assertion .
  dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance a np:Provenance .
  dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion {
  miriam-gene:2247 a ncit:C16612 .
  lld:C1168401 a ncit:C7057 .
  dgn-gda:DGN14b1690e337391923f6010615777d94e sio:SIO_000628 miriam-gene:2247 , lld:C1168401 ;
    a sio:SIO_001121 .
}
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance {
  dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion dcterms:description "[This study is to investigate if the FGF2-targeted adenoviral mutant Nijmegen breakage syndrome 1 (FGF2-Ad-NBS1) gene transfer can enhance cisplatin chemosensitisation not only by targeting DNA repair, but also through the induction of antiangiogenesis, whereas at the same time reducing toxicities in treating head and neck squamous cell carcinoma (HNSCC).]. 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:21063405 ;
    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:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}