@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI> .
@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:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_head {
  this: np:hasAssertion dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion;
    np:hasProvenance dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance;
    np:hasPublicationInfo dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion a np:Assertion .
  
  dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance a np:Provenance .
  
  dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0007102 a ncit:C7057 .
  
  dgn-gda:DGN70747abf6b5da30f7a48729b8167516b sio:SIO_000628 miriam-gene:4360, lld:C0007102;
    a sio:SIO_001121 .
}

dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance {
  dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion dcterms:description
      "[Deleterious germ-line variants involving the DNA mismatch repair (MMR) genes have been identified as the cause of the hereditary nonpolyposis colorectal cancer syndrome known as the Lynch syndrome, but in numerous familial clusters of colon cancer, the cause remains obscure.]. 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:21671081;
    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:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_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" .
}