Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion type Assertion NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_head.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_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." NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion evidence source_evidence_literature NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion SIO_000772 18080139 NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion wasDerivedFrom befree-2016 NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance.
- NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion wasGeneratedBy ECO_0000203 NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance.