@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE> .
@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:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_head {
  this: np:hasAssertion dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_assertion;
    np:hasProvenance dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_provenance;
    np:hasPublicationInfo dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_assertion a np:Assertion .
  
  dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_provenance a np:Provenance .
  
  dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN5c79b8339ea609761873224925c367b1 sio:SIO_000628 miriam-gene:4292, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_provenance {
  dgn-np:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_assertion dcterms:description
      "[The majority of HNPCC families have germline mutations in mismatch repair (MMR) genes, such as MSH2 or MLH1, so that HNPCC cancers characteristically exhibit DNA replication errors (RERs) at microsatellite loci.]. 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:9004127;
    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:NP1366021.RAjcFx-t6sIplPg8YeXrAZvzs_o4TS6gazwzcyKtSF_qE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:05+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" .
}