Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion type Assertion NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_head.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion description "[No other gene is present in the wasted deletion, and transgenic studies have shown that the phenotype is due to loss of eEF1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion evidence source_evidence_literature NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion SIO_000772 19909265 NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion wasDerivedFrom befree-20150227 NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_assertion wasGeneratedBy ECO_0000203 NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.