Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion type Assertion NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_head.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_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." NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_provenance.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion evidence source_evidence_literature NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_provenance.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion SIO_000772 22022284 NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_provenance.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion wasDerivedFrom befree-20140225 NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_provenance.
- NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_assertion wasGeneratedBy ECO_0000203 NP630895.RAwd9Cp1HXCzNUEFG0NbEuCGScTeLBInN7UjB2WRzlrfE130_provenance.