@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM> .
@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:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_head {
  this: np:hasAssertion dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_assertion;
    np:hasProvenance dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_provenance;
    np:hasPublicationInfo dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_assertion a np:Assertion .
  
  dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_provenance a np:Provenance .
  
  dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_assertion {
  miriam-gene:581 a ncit:C16612 .
  
  lld:C0699790 a ncit:C7057 .
  
  dgn-gda:DGNa3ac7ac8d666131a2a07bffb0cce2a39 sio:SIO_000628 miriam-gene:581, lld:C0699790;
    a sio:SIO_001121 .
}

dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_provenance {
  dgn-np:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_assertion dcterms:description
      "[This instability is reflected in a high mutation rate of microsatellites, and recent studies in colon cancer indicate that defects in MMR result in frequent frameshift mutations in mononucleotide repeats located in the coding regions of BAX and transforming growth factor-beta (TGF-beta) receptor genes.]. 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:9639521;
    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:NP800880.RAG-HtrnnLGAMwFo3qQebmnCCp3nmoiwDFmS2_IOAEbbM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}