@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY> .
@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:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_head {
  this: np:hasAssertion dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_assertion;
    np:hasProvenance dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_provenance;
    np:hasPublicationInfo dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_assertion a np:Assertion .
  
  dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_provenance a np:Provenance .
  
  dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN339bba720b382fea8b75f1cf91566368 sio:SIO_000628 miriam-gene:4360, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_provenance {
  dgn-np:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_assertion dcterms:description
      "[Lynch syndrome, an autosomal dominant cancer predisposition caused by mutations in DNA mismatch repair (MMR) genes, mainly mainly mutL homolog 1, OMIM 120436 (MLH1) and mutS homolog 2, OMIM 609309 (MSH2), encompasses a tumor spectrum including primarily gastrointestinal, endometrial, and ovarian cancer.]. 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:22034109;
    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:NP934275.RAwV6lrPmJCJOpPoyHL0hgWwhWr07NRC-XuXMiH9uxdoY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:48+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" .
}