Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion> ?p ?o ?g. }
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- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion type Assertion NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_head.
- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion wasGeneratedBy ECO_0000203 NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_provenance.
- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion wasDerivedFrom befree-20150227 NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_provenance.
- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion SIO_000772 22535952 NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_provenance.
- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion evidence source_evidence_literature NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_provenance.
- NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_assertion description "[Humans diagnosed with mutations in the gene NDUFS4, encoding a nuclear DNA-encoded subunit of CI (NADH dehydrogenase ubiquinone Fe-S protein 4), typically suffer from Leigh syndrome, a neurodegenerative disease with onset in infancy or early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775847.RAQvgsug9ML_BF1rm_U2vcQ7JPgTJ8FrlYHWVp6utchZg130_provenance.