Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_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." NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_assertion evidence source_evidence_literature NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_assertion SIO_000772 17327441 NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_assertion wasDerivedFrom befree-20150227 NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_assertion wasGeneratedBy ECO_0000203 NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP233034.RAAidCyN_K9_WEdN3uxZNi918NV1H_G8C-F87d12JfNrs130_provenance.