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- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_assertion type Assertion NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_head.
- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_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." NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_provenance.
- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_assertion evidence source_evidence_literature NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_provenance.
- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_assertion SIO_000772 21258814 NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_provenance.
- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_assertion wasDerivedFrom befree-20150227 NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_provenance.
- NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_assertion wasGeneratedBy ECO_0000203 NP868117.RAv3LOBJFngd2SmkEbBiKE5_aT6LXA3RYX7UydghRmYuY130_provenance.