@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo> .
@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:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_head {
  this: np:hasAssertion dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_assertion;
    np:hasProvenance dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_provenance;
    np:hasPublicationInfo dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_assertion a np:Assertion .
  
  dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_provenance a np:Provenance .
  
  dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_assertion {
  miriam-gene:3934 a ncit:C16612 .
  
  lld:C0022116 a ncit:C7057 .
  
  dgn-gda:DGNe8bb63ecb6246a91c6d2779430e1a606 sio:SIO_000628 miriam-gene:3934, lld:C0022116;
    a sio:SIO_001121 .
}

dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_provenance {
  dgn-np:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_assertion dcterms:description
      "[Inhibition of HDAC1 activity by p25/Cdk5 was identified as an underlying mechanism for these events, and HDAC1 gain of function provided potent protection against DNA damage and neurotoxicity in cultured neurons and an in vivo model for ischemia.]. 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:19081376;
    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:NP313790.RAD-eqn9Bn1INeVXytTmCXb31E36KxFDKBQB_Z8_C1GOo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:00+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" .
}