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- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion type Assertion NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_head.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion description "[All of our patients carried autosomal recessive mutations in ETFDH, suggesting that ETFDH deficiency leads to a secondary CoQ10 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion evidence source_evidence_literature NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion SIO_000772 17412732 NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion wasDerivedFrom befree-2016 NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.
- NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_assertion wasGeneratedBy ECO_0000203 NP603096.RA7YK19zJT-EkpNPOfLMHX6qMybHWLNkQxa6D5VkkQVGg130_provenance.