@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE> .
@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:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_head {
  this: np:hasAssertion dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion ;
    np:hasProvenance dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance ;
    np:hasPublicationInfo dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion a np:Assertion .
  dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance a np:Provenance .
  dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion {
  miriam-gene:5888 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGN5bd5c4fc4456373004c20d386fbf2930 sio:SIO_000628 miriam-gene:5888 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance {
  dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion dcterms:description "[Furthermore, with age of infection as an important factor in disease progression to HCC, results from the Cox proportional hazards analysis showed no significant associations between any of the tested RAD51 variants and the age of onset of HCC (P > 0.05), suggesting that genetic polymorphisms of RAD51 may not play an important role in clearance of HBV and disease progression to HCC.]. 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:21915862 ;
    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:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}