Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_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." NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_assertion evidence source_evidence_literature NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_assertion SIO_000772 18080139 NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_assertion wasDerivedFrom befree-20150227 NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_assertion wasGeneratedBy ECO_0000203 NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP759718.RAAqE9mxncoKFiqdWqrooJbuvJigrZCgOyirojkq2D5q8130_provenance.