@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU> .
@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/v3.0.0/void/> .
dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_head {
  this: np:hasAssertion dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_assertion ;
    np:hasProvenance dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_provenance ;
    np:hasPublicationInfo dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_assertion a np:Assertion .
  dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_provenance a np:Provenance .
  dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  lld:C0007103 a ncit:C7057 .
  dgn-gda:DGN584b07b1c76ea2f737523336459d8d00 sio:SIO_000628 miriam-gene:7515 , lld:C0007103 ;
    a sio:SIO_001122 .
}
dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_provenance {
  dgn-np:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_assertion dcterms:description "[The 751 Lys/Gln polymorphism of the ERCC2 gene may be linked with endometrial cancer occurrence and its effect can be potentiated by variants of the XRCC1 gene or first degree relatives positive cancer history.]. 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:22544315 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP779648.RA_wma5ozf6aMUeYiQDuP00yYxePk-Wx4i9irfRfzTjKU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:31+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}