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- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion type Assertion NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_head.
- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion description "[Furthermore, during the last decade, it has been identified that mutations in two mitochondrial fusion genes (MFN2 and OPA1) cause prevalent neurodegenerative diseases (Charcot-Marie Tooth type 2A and Kjer disease/autosomal dominant optic atrophy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_provenance.
- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion evidence source_evidence_literature NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_provenance.
- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion SIO_000772 19584314 NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_provenance.
- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion wasDerivedFrom befree-20150227 NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_provenance.
- NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_assertion wasGeneratedBy ECO_0000203 NP602691.RAttOAbTi2xNNJqK4s29jNvMt9Jigp3R5X0lNXnHJbq3E130_provenance.