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- source_evidence_literature type ECO_0000212 NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_assertion description "[To determine whether genetic variation in AKT2 plays a broader role in human metabolic disease, we sequenced the entire coding region and splice junctions of AKT2 in 94 unrelated patients with severe insulin resistance, 35 of whom had partial lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_assertion evidence source_evidence_literature NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_assertion SIO_000772 17327441 NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_assertion wasDerivedFrom befree-20150227 NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_assertion wasGeneratedBy ECO_0000203 NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP232985.RAmASrFnqefatkFae42mtQ7eEMBXbMr_iPdyW5zk5vvj8130_provenance.