@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_head {
  this: np:hasAssertion dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_assertion;
    np:hasProvenance dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_provenance;
    np:hasPublicationInfo dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_assertion a np:Assertion .
  
  dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_provenance a np:Provenance .
  
  dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_assertion {
  miriam-gene:999 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN05848e0758af929c77794466ff41ff7c sio:SIO_000628 miriam-gene:999, lld:C0027651;
    a sio:SIO_001122 .
}

dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_provenance {
  dgn-np:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_assertion dcterms:description
      "[In most hereditary cancer syndromes, like hereditory diffuse gastric cancer and lobular carcinoma of the breast, multiple organ sites are affected by cancer and have been shown to be associated with germline mutations in CDH1 at 16q22.1.]. 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:18046629;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP111542.RAW4D3KqYDU_rzju1EyXxuWyR9xXc0zi-tqZeVbVpYuAI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:57+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}