Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion> ?p ?o ?g. }
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- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion type Assertion NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_head.
- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_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." NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_provenance.
- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion evidence source_evidence_literature NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_provenance.
- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion SIO_000772 17327441 NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_provenance.
- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion wasDerivedFrom befree-20140225 NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_provenance.
- NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_assertion wasGeneratedBy ECO_0000203 NP638650.RAUqNsAqQqQxbklh9wMPOfoPzGagVR0CUTmo4h-3yL5VE130_provenance.