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- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_assertion type Assertion NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_head.
- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_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." NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_provenance.
- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_assertion evidence source_evidence_literature NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_provenance.
- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_assertion SIO_000772 19584314 NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_provenance.
- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_assertion wasDerivedFrom befree-20150227 NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_provenance.
- NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_assertion wasGeneratedBy ECO_0000203 NP832576.RAIKCOxsRAwwAGs-kZXwFA768G7SPWmRgBmQyB2DnLVi8130_provenance.