@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k> .
@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:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_head {
  this: np:hasAssertion dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_assertion;
    np:hasProvenance dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_provenance;
    np:hasPublicationInfo dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_assertion a np:Assertion .
  
  dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_provenance a np:Provenance .
  
  dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0476089 a ncit:C7057 .
  
  dgn-gda:DGNf0586ec6aa567b53398586c94c6c444b sio:SIO_000628 miriam-gene:4292, lld:C0476089;
    a sio:SIO_001121 .
}

dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_provenance {
  dgn-np:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_assertion dcterms:description
      "[As tumorigenesis in HNPCC is driven by deficient DNA mismatch repair (MMR), we compared its typical consequence, instability at microsatellite sequences, in colorectal and endometrial cancers from patients with identical predisposing mutations in the MMR genes MLH1 or MSH2.]. 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:12057899;
    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:NP176249.RARlCRDLLI2sU7a7MI4hhG3Xrbrxqaxlnl0Nk516LQC8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}