@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY> .
@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:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_head {
   this: np:hasAssertion dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_assertion ;
    np:hasProvenance dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_provenance ;
    np:hasPublicationInfo dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_assertion a np:Assertion .
  dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_provenance a np:Provenance .
  dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_assertion {
   miriam-gene:2068 a ncit:C16612 .
  lld:C0152018 a ncit:C7057 .
  dgn-gda:DGNb6926de8f750b4bfbe24cd740f2b3439 sio:SIO_000628 miriam-gene:2068 , lld:C0152018 ;
    a sio:SIO_001121 .
}
dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_provenance {
   dgn-np:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_assertion dcterms:description "[Genetic variants in ERCC2 and ERCC4 may provide further survival prediction in addition to TNM staging system of esophageal cancer, which is more evident in the patients with early disease status.]. 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:21490450 ;
    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:NP886926.RA-S0cuCfJy6F34C5g696zgstG1OKe7ExgUlQT8TQxbSY130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:26+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" .
}