@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0> .
@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:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_head {
  this: np:hasAssertion dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_assertion;
    np:hasProvenance dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_provenance;
    np:hasPublicationInfo dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_assertion a np:Assertion .
  
  dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_provenance a np:Provenance .
  
  dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_assertion {
  miriam-gene:10721 a ncit:C16612 .
  
  lld:C0043346 a ncit:C7057 .
  
  dgn-gda:DGN9b812cefdfce0c6eeb6bf885eaee9ca6 sio:SIO_000628 miriam-gene:10721, lld:C0043346;
    a sio:SIO_001121 .
}

dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_provenance {
  dgn-np:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_assertion dcterms:description
      "[To identify DNA polymerases that are involved in Ig gene conversion, we created DT40 clones deficient in DNA polymerase eta (poleta), which, in humans, is defective in the variant form of xeroderma pigmentosum (XP-V).]. 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:16337602;
    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:NP552697.RAG7qQdsz2olTRl9wQk92LpqzmSlDZUxkECaUj_tXcSi0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}