@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI> .
@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:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_head {
  this: np:hasAssertion dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_assertion ;
    np:hasProvenance dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_provenance ;
    np:hasPublicationInfo dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_assertion a np:Assertion .
  dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_provenance a np:Provenance .
  dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_assertion {
  miriam-gene:3981 a ncit:C16612 .
  lld:C0007137 a ncit:C7057 .
  dgn-gda:DGN8a181e5254b596641996667a408e019f sio:SIO_000628 miriam-gene:3981 , lld:C0007137 ;
    a sio:SIO_001121 .
}
dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_provenance {
  dgn-np:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_assertion dcterms:description "[An SNP, Arg72Pro, of the TP53 gene encoding a DNA damage response protein showed the strongest association with squamous cell carcinoma risk (OR Pro/Pro vs. Arg/Arg = 2.2), while 2 other SNPs, Phe257Ser of the REV gene encoding a translesion DNA polymerase and Ile658Val of the LIG4 gene encoding a DNA double-strand break repair protein, also showed associations (OR Ser/Ser vs. Phe/Phe = 2.0 and OR Ile/Val vs. Ile/Ile = 0.4, respectively).]. 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:15609317 ;
    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:NP606269.RAK0DPXcna4HvzMhbZbjpJ6LBqI7kqApMredFv90uESmI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:04+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" .
}