Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion type Assertion NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_head.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion wasGeneratedBy ECO_0000203 NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion wasDerivedFrom befree-20150227 NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion SIO_000772 15921863 NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion evidence source_evidence_literature NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.
- NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_assertion description "[In addition, recessive POLG1 mutations are responsible for sensory-atactic neuropathy, dysarthria and ophthalmoplegia (SANDO), juvenile spino-cerebellar ataxia-epilepsy syndrome (SCAE) and Alpers-Huttenlocher hepatopathic poliodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633482.RACmsrntkb5DWpnMr6ggN0jtEDurVUBSC19LYKAKu_rL4130_provenance.