@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw> .
@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:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_head {
  this: np:hasAssertion dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion;
    np:hasProvenance dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_provenance;
    np:hasPublicationInfo dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion a np:Assertion .
  
  dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_provenance a np:Provenance .
  
  dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN0d4f2393a115541f94bdbc40b182e17b sio:SIO_000628 miriam-gene:4360, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_provenance {
  dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion dcterms:description
      "[We found no evidence that the SNPs associated with CRC in the general population are modifiers of the risk for MMR gene mutation carriers overall, and therefore any evidence of proven clinical utility in 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:23434150;
    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:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:44+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" .
}