Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion> ?p ?o ?g. }
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- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion type Assertion NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_head.
- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_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." NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_provenance.
- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion evidence source_evidence_literature NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_provenance.
- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion SIO_000772 19584314 NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_provenance.
- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion wasDerivedFrom befree-20140225 NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_provenance.
- NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_assertion wasGeneratedBy ECO_0000203 NP535024.RAUGkOryOS7fFpn_CXUfv2kx33EhV-C_fwJVgXhYNXQsI130_provenance.