@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:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_head { this: np:hasAssertion dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_assertion; np:hasProvenance dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_provenance; np:hasPublicationInfo dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_publicationInfo; a np:Nanopublication . dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_assertion a np:Assertion . dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_provenance a np:Provenance . dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_publicationInfo a np:PublicationInfo . } dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_assertion { miriam-gene:9968 a ncit:C16612 . lld:C0338508 a ncit:C7057 . dgn-gda:DGN3b90ba0934fcdcc05319fe37249254cc sio:SIO_000628 miriam-gene:9968, lld:C0338508; a sio:SIO_001121 . } dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_provenance { dgn-np:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_assertion dcterms:description "[To characterize the molecular links between type-1 autosomal dominant optic atrophy (ADOA) and OPA1 dysfunctions, the effects of pathogenic alleles of this dynamin on mitochondrial morphology and apoptosis were analyzed, either in fibroblasts from affected individuals, or in HeLa cells transfected with similar mutants.]. 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:17167772; 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:NP584244.RAwp0H5h5O0mxBPnx4A6tARQ9TmCDnrFxrfUgk3BAsdek130_publicationInfo { this: dcterms:created "2016-05-13T12:46:10+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" . }