Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion> ?p ?o ?g. }
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- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion type Assertion NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_head.
- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion wasGeneratedBy ECO_0000203 NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_provenance.
- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion wasDerivedFrom befree-20140225 NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_provenance.
- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion SIO_000772 21362476 NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_provenance.
- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion evidence source_evidence_literature NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_provenance.
- NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_assertion description "[To see if ATP13A2 mutations could be responsible for some cases of human adult-onset NCL (Kufs disease), we resequenced ATP13A2 from 28 Kufs disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776504.RATChd7L22w4fLLG4PWCql1P9HZOXI-95Vy-ugZIUxc7Q130_provenance.