@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU> .
@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/v3.0.0/void/> .

dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_head {
  this: np:hasAssertion dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion;
    np:hasProvenance dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance;
    np:hasPublicationInfo dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion a np:Assertion .
  
  dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance a np:Provenance .
  
  dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1306459 a ncit:C7057 .
  
  dgn-gda:DGNf0d84fe691a71853f5566ac98c41dc5d sio:SIO_000628 miriam-gene:4360, lld:C1306459;
    a sio:SIO_001121 .
}

dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_provenance {
  dgn-np:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_assertion dcterms:description
      "[In many individuals suspected of the common cancer predisposition Lynch syndrome, variants of unclear significance (VUS), rather than an obviously pathogenic mutations, are identified in one of the DNA mismatch repair (MMR) genes.]. 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:23690608;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP568806.RAvnyD6b48Q14Sjf-Vpzh1QV-ya-NYMJILfPjnmeQiHkU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:18+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}