@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc> .
@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:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_head {
  this: np:hasAssertion dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_assertion;
    np:hasProvenance dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_provenance;
    np:hasPublicationInfo dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_assertion a np:Assertion .
  
  dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_provenance a np:Provenance .
  
  dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNd4d24f95a76144e35ec27ddbb599d5af sio:SIO_000628 miriam-gene:4360, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_provenance {
  dgn-np:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_assertion dcterms:description
      "[To evaluate our experience of adding reflex BRAF mutation analysis following mismatch repair (MMR) protein staining in the test algorithm for Lynch syndrome (LS), the most common inherited predisposition to colorectal cancer (CRC).]. 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:23897252;
    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:NP1097919.RAnHdSKCdouiEXcBXQXXz1DCCd0A5ZcJUecg1QgTmxlWc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:03+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" .
}