Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion> ?p ?o ?g. }
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- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion type Assertion NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_head.
- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion description "[Mutations in the gene mitofusin 2 (MFN2) cause the axonal subtype CMT2A, which has also been shown to be associated with optic atrophy, clinical signs of first motor neuron involvement, and early onset stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_provenance.
- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion evidence source_evidence_literature NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_provenance.
- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion SIO_000772 21258814 NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_provenance.
- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion wasDerivedFrom befree-2016 NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_provenance.
- NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_assertion wasGeneratedBy ECO_0000203 NP867197.RAR_DCMTOLIFYAQEQHL2yr-ieUnqumDFeYW1PLIpBCo-Q130_provenance.