Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion> ?p ?o ?g. }
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- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion type Assertion NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_head.
- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_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." NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_provenance.
- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion evidence source_evidence_literature NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_provenance.
- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion SIO_000772 19584314 NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_provenance.
- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion wasDerivedFrom befree-20140225 NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_provenance.
- NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_assertion wasGeneratedBy ECO_0000203 NP483252.RAkT1X3zwW1d1_OsyIjW3hs3fKOIUmu3QkAxBHCtu5H8k130_provenance.