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- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion type Assertion NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_head.
- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion wasGeneratedBy ECO_0000203 NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_provenance.
- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion wasDerivedFrom befree-20140225 NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_provenance.
- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion SIO_000772 23108404 NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_provenance.
- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion evidence source_evidence_literature NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_provenance.
- NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_assertion description "[Hyperactive mTOR signaling due to the loss-of-function of mutations in either TSC1 or TSC2 gene causes TSC, an autosomal dominant disorder featured with benign tumors in multiple organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858219.RAi2H1gtS00B4kIFuNWZVu-GQbESmUQ9M5l79B3mhtCa8130_provenance.