Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion> ?p ?o ?g. }
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- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion type Assertion NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_head.
- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion description "[We previously reported a family in which a heterozygous missense mutation in Akt2 led to a dominantly inherited syndrome of insulin-resistant diabetes and partial lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_provenance.
- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion evidence source_evidence_literature NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_provenance.
- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion SIO_000772 17327441 NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_provenance.
- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion wasDerivedFrom befree-20150227 NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_provenance.
- NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_assertion wasGeneratedBy ECO_0000203 NP233101.RAOyElwHQVVw_u7m3mR8JJckY_fmoJtLh8McnwxcGX-bk130_provenance.