Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion> ?p ?o ?g. }
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- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion type Assertion NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_head.
- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_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." NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_provenance.
- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion evidence source_evidence_literature NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_provenance.
- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion SIO_000772 18080139 NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_provenance.
- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion wasDerivedFrom befree-20150227 NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_provenance.
- NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_assertion wasGeneratedBy ECO_0000203 NP758842.RAfjTq0ezTC9znUTmuTLpXC1ZQec6k5XRb9co27SFPfls130_provenance.