Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion> ?p ?o ?g. }
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- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion type Assertion NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_head.
- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_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." NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_provenance.
- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion evidence source_evidence_literature NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_provenance.
- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion SIO_000772 19584314 NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_provenance.
- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion wasDerivedFrom befree-2016 NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_provenance.
- NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_assertion wasGeneratedBy ECO_0000203 NP749982.RApm-GIwqZqr9rn_pA0UqOZfUNoPv-H3DFirFDW_zIOiw130_provenance.