@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:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_head { this: np:hasAssertion dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_assertion; np:hasProvenance dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_provenance; np:hasPublicationInfo dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_assertion a np:Assertion . dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_provenance a np:Provenance . dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_assertion { miriam-gene:1832 a ncit:C16612 . lld:C0349788 a ncit:C7057 . dgn-gda:DGNfbfaccb7788780ac576d8c642b0d71b0 sio:SIO_000628 miriam-gene:1832, lld:C0349788; a sio:SIO_001121 . } dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_provenance { dgn-np:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_assertion dcterms:description "[Here, we show that iASPP is expressed at intercalated discs in human and mouse postmitotic cardiomyocytes. iASPP interacts with desmoplakin and desmin in cardiomyocytes to maintain the integrity of desmosomes and intermediate filament networks in vitro and in vivo. iASPP deficiency specifically induces right ventricular dilatation in mouse embryos at embryonic day 16.5. iASPP-deficient mice with exon 8 deletion (Ppp1r13l(Δ8/Δ8)) die of sudden cardiac death, displaying features of ARVC.]. 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:25691752; 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:NP1264528.RAejDW9G2SIhSsSsfIf2shvMKMR5itdGoCmM6KzKiYTPQ130_publicationInfo { this: dcterms:created "2016-05-13T12:51:19+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" . }