@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis> .
@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:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_head {
  this: np:hasAssertion dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_assertion;
    np:hasProvenance dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_provenance;
    np:hasPublicationInfo dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_assertion a np:Assertion .
  
  dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_provenance a np:Provenance .
  
  dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_assertion {
  miriam-gene:2956 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN744c279e2c9c7b326d4cefc7121ca833 sio:SIO_000628 miriam-gene:2956, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_provenance {
  dgn-np:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_assertion dcterms:description
      "[In conclusion, our data outline the main scenarios where significant reduction of MSH6 staining is more likely to occur in colorectal carcinoma, and suggest that somatic mutations of the coding region microsatellites of the MSH6 gene is an underlying mechanism for this staining phenomenon in MLH1/PMS2-deficient carcinomas.]. 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:22918162;
    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:NP287193.RATgzIlpGOWXhvcavig9GHAhO8F6GA01rIMl-VCJa-Bis130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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" .
}