@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU> .
@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:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_head {
  this: np:hasAssertion dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_assertion;
    np:hasProvenance dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_provenance;
    np:hasPublicationInfo dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_assertion a np:Assertion .
  
  dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_provenance a np:Provenance .
  
  dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNd48f8fd74ba8a3c1b62baa7f7556de0e sio:SIO_000628 miriam-gene:4292, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_provenance {
  dgn-np:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_assertion dcterms:description
      "[Mutations affecting human mismatch repair (MMR) genes (MLH1, MSH2, PMS1, PMS2, and MSH6) cause tumour predisposition in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome, and an association has been demonstrated with the replication error (RER) phenotype in most colorectal and some extracolonic neoplasms.]. 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:10448273;
    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:NP288461.RAFEUpdBfIXSvHl74hUbvgPRbW-6LpvnMMl4fzKQsFpLU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}