@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs> .
@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:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_head {
  this: np:hasAssertion dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion;
    np:hasProvenance dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance;
    np:hasPublicationInfo dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion a np:Assertion .
  
  dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance a np:Provenance .
  
  dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion {
  miriam-gene:11200 a ncit:C16612 .
  
  lld:C1458155 a ncit:C7057 .
  
  dgn-gda:DGNf933dfb7dfae2a540395773fed5df692 sio:SIO_000628 miriam-gene:11200, lld:C1458155;
    a sio:SIO_001122 .
}

dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance {
  dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion dcterms:description
      "[We believe that CHEK2 mutations are not associated with the cancer types seen in the LFS or LFL (other than breast cancer) and it is no longer reasonable to consider CHEK2 mutations to be a cause of LFS (Li-Fraumeni syndrome).]. 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:18178638;
    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:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:55+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" .
}