Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_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." NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_assertion evidence source_evidence_literature NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_assertion SIO_000772 17327441 NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_assertion wasDerivedFrom befree-2016 NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_assertion wasGeneratedBy ECO_0000203 NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.
- befree-2016 importedOn "2016-02-19" NP596250.RAFFIJyFYkWt_FdGCPbvQA_K1b48qquce5njVefhwHi3o130_provenance.