@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g> .
@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:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_head {
  this: np:hasAssertion dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_assertion;
    np:hasProvenance dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_provenance;
    np:hasPublicationInfo dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_assertion a np:Assertion .
  
  dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_provenance a np:Provenance .
  
  dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_assertion {
  miriam-gene:2956 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN0865dd7d7fc3a2b4550f42c928e93618 sio:SIO_000628 miriam-gene:2956, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_provenance {
  dgn-np:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_assertion dcterms:description
      "[Immunohistochemistry (MLH1, MSH2, MSH6) showed that loss of mismatch repair protein expression occurred in all MSI UUC defining the gene defect and that MRE11 and RAD50 mutations were associated with their concomitant loss expression.]. 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:16288216;
    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:NP593907.RA47Lne2qv_aafZYuFi-15mvz7YVF0JEUjULD60eWu26g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:57+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" .
}