@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM> .
@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:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_head {
  this: np:hasAssertion dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion;
    np:hasProvenance dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance;
    np:hasPublicationInfo dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion a np:Assertion .
  
  dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance a np:Provenance .
  
  dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion {
  miriam-gene:841 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN5136586a7430d442dbe03fae161b2a87 sio:SIO_000628 miriam-gene:841, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_provenance {
  dgn-np:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_assertion dcterms:description
      "[Our findings suggest that methylation commonly contributes to CASP8 silencing in medulloblastomas and that homozygous deletion or severe sequence changes involving the promoter region may be another mechanism leading to CASP8 inactivation in this neoplasm.]. 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:15289853;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP586137.RAL_6N8vbrJacCt4FRafSbG5AXNAr0kT9Hy9iuzGMRScM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}