@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_head { this: np:hasAssertion dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_assertion; np:hasProvenance dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_provenance; np:hasPublicationInfo dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_publicationInfo; a np:Nanopublication . dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_assertion a np:Assertion . dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_provenance a np:Provenance . dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_publicationInfo a np:PublicationInfo . } dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_assertion { miriam-gene:1387 a ncit:C16612 . lld:C0035934 a ncit:C7057 . dgn-gda:DGN510563cb12f59f5ff22834c61a849a4e sio:SIO_000628 miriam-gene:1387, lld:C0035934; a sio:SIO_001121 . } dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_provenance { dgn-np:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_assertion dcterms:description "[The comparison of CREBBP-mutated RSTS cell lines with cell lines derived from patients with an unrelated mental retardation syndrome or healthy controls revealed significant deficits in histone acetylation, affecting primarily histone H2B and histone H2A.]. 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:21984751; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP929669.RAbmXTLDLKXE8HSaMolPrjsC6PElMbxtPdBvpoBiYY0sg130_publicationInfo { this: dcterms:created "2016-05-13T12:48:46+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }