Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_assertion description "[OPA1 (Optic Atrophy-1) is involved in fusion of mitochondrial inner membrane, and its heterozygous mutations lead to early-onset and progressive dominant optic atrophy which may be complicated by other neurological symptoms including peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_assertion evidence source_evidence_literature NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_assertion SIO_000772 25847151 NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_assertion wasDerivedFrom befree-2016 NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_assertion wasGeneratedBy ECO_0000203 NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1276204.RApIqsluWBntMqna9T2Hle1tw_NHQOKSBYI5edizqmSD8130_provenance.