Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion> ?p ?o ?g. }
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- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion type Assertion NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_head.
- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion description "[Inactivating mutations in the serine-threonine kinase LKB1 (STK11) are found in most patients with Peutz-Jeghers syndrome; however the function of LKB1 is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion evidence source_evidence_literature NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion SIO_000772 11445556 NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion wasDerivedFrom befree-2016 NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_assertion wasGeneratedBy ECO_0000203 NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.