Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion type Assertion NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_head.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_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." NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_provenance.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion evidence source_evidence_literature NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_provenance.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion SIO_000772 19584314 NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_provenance.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion wasDerivedFrom befree-2016 NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_provenance.
- NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_assertion wasGeneratedBy ECO_0000203 NP749983.RACLvylC_mvhU6o2GIzI_dfE__IarplTbPLEmqGE4IfTU130_provenance.