@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg> .
@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:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_head {
  this: np:hasAssertion dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion;
    np:hasProvenance dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance;
    np:hasPublicationInfo dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion a np:Assertion .
  
  dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance a np:Provenance .
  
  dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN88c3ae96ef4aafdd47c749f245970065 sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance {
  dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion dcterms:description
      "[Due to the minor role of germline MSH6 mutations, we adapted the Lynch syndrome detection strategy for the Slovenian population of CRC patients, whereby germline alterations should be first sought in MLH1 and MSH2 followed by a search for larger genomic rearrangements in these two 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:19526325;
    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:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:23+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" .
}