Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_assertion wasGeneratedBy ECO_0000203 NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_assertion wasDerivedFrom befree-2016 NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_assertion SIO_000772 21428921 NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_assertion evidence source_evidence_literature NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.
- NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_assertion description "[Mutations in genes encoding either hamartin [TSC1 (tuberous sclerosis complex 1)] or tuberin (TSC2) result in a multisystem disorder characterized by the development of benign tumours and hamartomas in several organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881658.RA8b0Zcb7JdYMebrybYiEiElIf1Ltm2NFioN58HesTpn0130_provenance.