@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ> .
@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:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_head {
  this: np:hasAssertion dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_assertion;
    np:hasProvenance dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_provenance;
    np:hasPublicationInfo dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_assertion a np:Assertion .
  
  dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_provenance a np:Provenance .
  
  dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0279672 a ncit:C7057 .
  
  dgn-gda:DGNcc9984f481b7e797993e08f10cdb879c sio:SIO_000628 miriam-gene:7157, lld:C0279672;
    a sio:SIO_001121 .
}

dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_provenance {
  dgn-np:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_assertion dcterms:description
      "[The aims of this study were to evaluate the genotype frequencies of p53 codon 72 and p21 codon 31 in cervical adenocarcinoma patients and controls, and the association between the specific genotype or genotype combination of these polymorphisms and the risk of cervical adenocarcinoma in Korean women.]. 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:20524403;
    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:NP637135.RARUDiFts-5Dp3mW4ByUPrRXA7Rw3ZkF9e_sJc0T3V_NQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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" .
}