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- source_evidence_literature type ECO_0000212 NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP366270.RAUdOb9RE7Nu404de_XKvuG-pDgSYeF_9AedKxu_Spedc130_provenance.