Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_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." NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_assertion evidence source_evidence_literature NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_assertion SIO_000772 12906785 NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_assertion wasDerivedFrom befree-2016 NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_assertion wasGeneratedBy ECO_0000203 NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.
- befree-2016 importedOn "2016-02-19" NP404689.RAyaLKofw0CbPBI1dG0Re2WJyIjDsZntkNFMz5UvrDJkM130_provenance.