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- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion type Assertion NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_head.
- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion wasGeneratedBy ECO_0000203 NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.
- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion wasDerivedFrom befree-20140225 NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.
- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion SIO_000772 16919951 NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.
- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion evidence source_evidence_literature NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.
- NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_assertion description "[Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493110.RATi9C6QF0Jmle_PhyVLu3NAuixZt0QQ0GvlAJwjfoZ_I130_provenance.