@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI> .
@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:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_head {
  this: np:hasAssertion dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_assertion ;
    np:hasProvenance dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_provenance ;
    np:hasPublicationInfo dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_assertion a np:Assertion .
  dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_provenance a np:Provenance .
  dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  lld:C0596263 a ncit:C7057 .
  dgn-gda:DGN7ae83bb3825f4d918d5b1dacc73af1b7 sio:SIO_000628 miriam-gene:4292 , lld:C0596263 ;
    a sio:SIO_001122 .
}
dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_provenance {
  dgn-np:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_assertion dcterms:description "[These data confirm that functional deficiencies in the interaction of hMLH1 with hPMS2 are associated with HNPCC as well as suggest that other unknown functional alteration of the human MutL homologues may lead to tumorigenesis in HNPCC kindreds.]. 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:10037723 ;
    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:NP246503.RA2B_bwyIr5l1fOV-lWOb4onG0QVJrm-N83M0ONMQboFI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:38+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}