Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion> ?p ?o ?g. }
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- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion type Assertion NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_head.
- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion description "[Tuberous Sclerosis Complex (TSC) is a genetic disorder that occurs through the loss of heterozygosity of either TSC1 or TSC2, which encode Hamartin or Tuberin, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_provenance.
- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion evidence source_evidence_literature NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_provenance.
- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion SIO_000772 12906785 NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_provenance.
- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion wasDerivedFrom befree-20140225 NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_provenance.
- NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_assertion wasGeneratedBy ECO_0000203 NP606558.RAKJyjtoQ8O_iPwdE9myiUZngGVQTVZBbzyb3r9SlzXWM130_provenance.