Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion> ?p ?o ?g. }
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- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion type Assertion NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_head.
- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion description "[Finally, discovery of a shared activation of the hypoxic response in pheochromocytomas with mutations in VHL and SDH genes and uncovering of a common JunB-mediated apoptosis defect in the major hereditary groups of pheochromocytoma have provided a mechanistic basis for the clinical similarities between these distinct syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_provenance.
- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion evidence source_evidence_literature NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_provenance.
- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion SIO_000772 16357557 NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_provenance.
- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion wasDerivedFrom befree-20140225 NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_provenance.
- NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_assertion wasGeneratedBy ECO_0000203 NP414141.RASIvC7VJA8bUmPJxbAylTcVAv7AWEWtttH4LZW4yLZA0130_provenance.