@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg> .
@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:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_head {
  this: np:hasAssertion dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_assertion;
    np:hasProvenance dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_provenance;
    np:hasPublicationInfo dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_assertion a np:Assertion .
  
  dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_provenance a np:Provenance .
  
  dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_assertion {
  miriam-gene:9407 a ncit:C16612 .
  
  lld:C0032339 a ncit:C7057 .
  
  dgn-gda:DGNec8591222fa2498fe69e10331d9b6c7a sio:SIO_000628 miriam-gene:9407, lld:C0032339;
    a sio:SIO_001121 .
}

dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_provenance {
  dgn-np:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_assertion dcterms:description
      "[These findings therefore underscore the functional importance of the PHD finger in vivo and imply that reduction of CBP HAT activity, as exemplified here by disruption of the PHD finger, is sufficient to cause RTS.]. 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:12566391;
    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:NP863009.RAthqGiY0-cfD_eYdLdc6j7q2x52v_DnZR62XaJD7nxKg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}