Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_assertion description "[Tuberous sclerosis complex (TSC) is a genetic disorder associated with mTOR over-activation and disruption of MAPK, PI3K and AMPK signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_assertion evidence source_evidence_literature NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_assertion SIO_000772 21191642 NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_assertion wasDerivedFrom befree-20150227 NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_assertion wasGeneratedBy ECO_0000203 NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP620989.RAE2rurq-IN_hiVVD7FIQYEcPn3PFfAR-rJUvp9ZGx0fM130_provenance.