@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:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_head { this: np:hasAssertion dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_assertion; np:hasProvenance dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_provenance; np:hasPublicationInfo dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_publicationInfo; a np:Nanopublication . dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_assertion a np:Assertion . dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_provenance a np:Provenance . dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_publicationInfo a np:PublicationInfo . } dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_assertion { miriam-gene:3416 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGN9744180f4ef547e4156aaa37678b3f49 sio:SIO_000628 miriam-gene:3416, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_provenance { dgn-np:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_assertion dcterms:description "[We conclude that naturally occurring, partial loss-of-function mutations in IDE sufficient to cause DM2 also impair neuronal regulation of Abeta levels, but the brain can apparently compensate for the partial deficit during the life span of the rat.]. 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:15039230; 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:NP436806.RAOSJMxfUWi1YKOV5qBPkWwOt2uCeOmEYeMVKDj_pzV6w130_publicationInfo { this: dcterms:created "2016-05-13T12:45:03+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" . }