Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_assertion description "[PEComas are related to the genetic alterations of tuberous sclerosis complex (TSC), an autosomal dominant genetic disease due to losses of TSC1 (9q34) or TSC2 (16p13.3) genes which seem to have a role in the regulation of the Rheb/mTOR/p70S6K pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_assertion evidence source_evidence_literature NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_assertion SIO_000772 18080139 NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_assertion wasDerivedFrom befree-20140225 NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_assertion wasGeneratedBy ECO_0000203 NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191029.RAQSbVwV5JJWH7o1ZgFDDV0xsgSB-oS5F0vMsTWr-5cWs130_provenance.