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- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion type Assertion NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_head.
- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion wasGeneratedBy ECO_0000203 NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_provenance.
- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion wasDerivedFrom befree-2016 NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_provenance.
- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion SIO_000772 19451219 NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_provenance.
- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion evidence source_evidence_literature NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_provenance.
- NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_assertion description "[Additionally, our Cisd2 knockout mouse work provides strong evidence supporting an earlier clinical hypothesis that WFS is in part a mitochondria-mediated disorder; specifically, we propose that mutation of CISD2 causes the mitochondria-mediated disorder WFS2 in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739775.RADESF3MKJq7qfRPbSAnDsqrlKBcryDWqzeAdOTkCfav0130_provenance.