Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion> ?p ?o ?g. }
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- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion type Assertion NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_head.
- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_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." NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance.
- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion evidence source_evidence_literature NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance.
- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion SIO_000772 17327441 NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance.
- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion wasDerivedFrom befree-20140225 NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance.
- NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_assertion wasGeneratedBy ECO_0000203 NP829529.RAxgMN3ZGibWJ9MUzpWPpCstZZ1hHutQVXH06diqnioa8130_provenance.