Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP323369.RAj1S98KdO8X1qdzLxOHDuXv90JUjTkQ71qi77QZIvCLM130_provenance.