@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo> .
@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:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_head {
  this: np:hasAssertion dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_assertion;
    np:hasProvenance dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_provenance;
    np:hasPublicationInfo dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_assertion a np:Assertion .
  
  dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_provenance a np:Provenance .
  
  dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_assertion {
  miriam-gene:5395 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN12f953636196396de554c5aacc737549 sio:SIO_000628 miriam-gene:5395, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_provenance {
  dgn-np:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_assertion dcterms:description
      "[The high frequency of MLH1 germline mutations identified in our study has important implications for testing strategies in patients suspected of having Lynch syndrome and indicates that patients with tumors demonstrating isolated loss of PMS2 expression without a germline PMS2 mutation must have MLH1 mutation analysis performed.]. 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:25871621;
    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:NP1277709.RAq4wCE8MK65lvPhto8rFS3Wc0qj6HvXAgIgW2W3kXrmo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:25+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" .
}