@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:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_head { this: np:hasAssertion dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_assertion; np:hasProvenance dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_provenance; np:hasPublicationInfo dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_publicationInfo; a np:Nanopublication . dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_assertion a np:Assertion . dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_provenance a np:Provenance . dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_publicationInfo a np:PublicationInfo . } dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_assertion { miriam-gene:5649 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN315c2e720666bd6f0966b9f7a3635f11 sio:SIO_000628 miriam-gene:5649, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_provenance { dgn-np:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_assertion dcterms:description "[The highly integrated layers of the epigenome are responsible for the cell type specific and exquisitely environmentally responsive deployment of genes and functional gene networks that underlie the molecular pathophysiology of epilepsy and its associated comorbidities, including but not limited to neurotransmitter receptors (e.g., GluR2, GLRA2, and GLRA3), growth factors (e.g., BDNF), extracellular matrix proteins (e.g., RELN), and diverse transcriptional regulators (e.g., CREB, c-fos, and c-jun).]. 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:20188170; 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:NP394194.RAAtUSaqT-4-Ll5izhBrJKUqpV-WcFxsc5oM7t1KaJ0R0130_publicationInfo { this: dcterms:created "2014-10-02T12:35:54+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }