@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI> .
@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:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_head {
  this: np:hasAssertion dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_assertion;
    np:hasProvenance dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_provenance;
    np:hasPublicationInfo dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_assertion a np:Assertion .
  
  dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_provenance a np:Provenance .
  
  dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_assertion {
  miriam-gene:5395 a ncit:C16612 .
  
  lld:C0685938 a ncit:C7057 .
  
  dgn-gda:DGNc0232ab9499015635ed0441fcfded96f sio:SIO_000628 miriam-gene:5395, lld:C0685938;
    a sio:SIO_001121 .
}

dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_provenance {
  dgn-np:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_assertion dcterms:description
      "[Among 70 gastrointestinal tract cancers (3 from the small bowel, 36 from the right colon, 15 from the left colon, and 16 from the anorectum), both the biopsy and resection specimens detected the same 29 cancers as having loss of staining for at least 1 protein, 14 affecting MLH1/PMS2 and 15 affecting MSH2/MSH6.]. 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:21297438;
    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:NP889202.RApDLL_E8C4HyGyCVPh8wb2EPVgG0JRZFTZjsANOb7QsI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:06+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" .
}