@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ> .
@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:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_head {
  this: np:hasAssertion dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_assertion;
    np:hasProvenance dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_provenance;
    np:hasPublicationInfo dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_assertion a np:Assertion .
  
  dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_provenance a np:Provenance .
  
  dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_assertion {
  miriam-gene:7376 a ncit:C16612 .
  
  lld:C0027126 a ncit:C7057 .
  
  dgn-gda:DGN45195279c1535275476a49a332d42718 sio:SIO_000628 miriam-gene:7376, lld:C0027126;
    a sio:SIO_001121 .
}

dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_provenance {
  dgn-np:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_assertion dcterms:description
      "[The influence of nucleotide excision repair (NER), the principal in vivo repair system for DNA damages, was investigated in Escherichia coli with uvrA, uvrB and uvrAuvrB mutants with the triplet repeat sequences (TRS) involved in myotonic dystrophy, the fragile X syndrome and Friedreich's ataxia.]. 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:9862988;
    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:NP826756.RAV9Ui29c1S-to8946KVNer5yyHTQQu17LLzDiPrEYRnQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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: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" .
}