Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion> ?p ?o ?g. }
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- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion type Assertion NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_head.
- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion description "[Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_provenance.
- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion evidence source_evidence_literature NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_provenance.
- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion SIO_000772 22022284 NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_provenance.
- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion wasDerivedFrom befree-20140225 NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_provenance.
- NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_assertion wasGeneratedBy ECO_0000203 NP795798.RAjcrCqdWK0SLVAVP62PoV6rr0DiTVOQDHbINRc37oWnE130_provenance.