@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_head {
  this: np:hasAssertion dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion;
    np:hasProvenance dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance;
    np:hasPublicationInfo dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion a np:Assertion .
  
  dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance a np:Provenance .
  
  dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGNbc2f2cf3c0b6522c4abc217a8478e860 sio:SIO_000628 miriam-gene:4436, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_provenance {
  dgn-np:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_assertion dcterms:description
      "[A significant fraction of hereditary nonpolyposis colorectal cancer cases with defective mismatch repair (ie, Lynch syndrome) have large genomic deletions or duplications in the mismatch repair genes, hMLH1 and hMSH2, which can be challenging to detect by traditional methods.]. 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:15858146;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP491953.RAOa_nld3VTofc8LZG1aXfMtgP4onLRbBq9a__ym2nx1k130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}