@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:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_head { this: np:hasAssertion dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_assertion; np:hasProvenance dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_provenance; np:hasPublicationInfo dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_publicationInfo; a np:Nanopublication . dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_assertion a np:Assertion . dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_provenance a np:Provenance . dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_assertion { miriam-gene:3481 a ncit:C16612 . lld:C0012236 a ncit:C7057 . dgn-gda:DGN427d434b1322b4974790221fbd54de7c sio:SIO_000628 miriam-gene:3481, lld:C0012236; a sio:SIO_001121 . } dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_provenance { dgn-np:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_assertion dcterms:description "[Here, we would like to review the rapidly growing world of IGF2 in cognitive neuroscience and introduce the evidence that its deficit is indeed involved in the impairment of the hippocampal neurogenesis and cognitive dysfunction in the model mouse of 22q11.2 deletion syndrome, which deletes Dgcr8, a critical gene for microRNA processing.]. 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:24778346; 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:NP1177660.RAK8Yc2KjGAw_aHcQciEV0mTmhAHKlWiWLyAR3f4Efht0130_publicationInfo { this: dcterms:created "2016-05-13T12:50:39+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" . }