@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM> .
@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:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_head {
  this: np:hasAssertion dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion;
    np:hasProvenance dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance;
    np:hasPublicationInfo dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion a np:Assertion .
  
  dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance a np:Provenance .
  
  dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN53bb5ab7ace417fb37bd1cde7a41d262 sio:SIO_000628 miriam-gene:4360, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_provenance {
  dgn-np:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_assertion dcterms:description
      "[Carcinomas of the small intestine are rare, but the risk is greatly increased in patients with hereditary nonpolyposis colorectal cancer (HNPCC) due to an inherited mismatch repair (MMR) gene mutation, most commonly affecting the genes MLH1 or MSH2.]. 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:12627520;
    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:NP386370.RA15afNcZH0IdAEzq4wgIN4iIaxemnXKjEGHND43EoeFM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:40+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" .
}