@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:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_head { this: np:hasAssertion dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_assertion; np:hasProvenance dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_provenance; np:hasPublicationInfo dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_publicationInfo; a np:Nanopublication . dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_assertion a np:Assertion . dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_provenance a np:Provenance . dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_publicationInfo a np:PublicationInfo . } dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_assertion { miriam-gene:9968 a ncit:C16612 . lld:C0029124 a ncit:C7057 . dgn-gda:DGN94a17082a24c8966812ec0a38bd1a49e sio:SIO_000628 miriam-gene:9968, lld:C0029124; a sio:SIO_001121 . } dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_provenance { dgn-np:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_assertion dcterms:description "[The study of the various clinical presentations of ADOA in conjunction with the investigation of OPA1 mutations in fibroblasts from patients with optic atrophy provides new insights into the pathophysiological mechanisms of the disease while underscoring the multiple physiological roles played by OPA1 in energetic metabolism, mitochondrial structure and maintenance, and cell death.]. 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:19389487; 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:NP734318.RACC7xTl1WXijrXQFtaQca06aPQDcbu9ZtPNOS0gw-AHc130_publicationInfo { this: dcterms:created "2016-05-13T12:47:18+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" . }