@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M> .
@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:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_head {
  this: np:hasAssertion dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion;
    np:hasProvenance dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance;
    np:hasPublicationInfo dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion a np:Assertion .
  
  dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance a np:Provenance .
  
  dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN593cb8b9a3d4bc81cd06679ea5884387 sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance {
  dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion dcterms:description
      "[Four of the 28 MSI-H cases, including one Amsterdam criteria case, had biallelic tumor MLH1 methylation, indicating that sporadic cases can be admixed in with Lynch syndrome cases, even those meeting the strongest criteria for Lynch syndrome.]. 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:19690142;
    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:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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" .
}