Hi Roberto,
As Dexter noted, the large corpus is a subset of the Selventa knowledge base. It is essentially a collection of independent facts – I don’t believe it was selected to represent any specific biological process(es) or signaling pathway(s). The RCR methods paper (http://www.biomedcentral.com/1471-2105/14/340) has some information about the contents of the large corpus since it used this corpus as a knowledge source. In particular, the supplemental data section provides a file listing the “mechanisms” (upstream controllers of multiple RNAs) that could be generated from the large corpus.
Best,
Natalie
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Roberto,
Great catch! Please go ahead and submit a Pull Request to the https://github.com/OpenBEL/openbel-framework-resources repository and we'll merge it in.
In the future feel free to open an issue and submit a Pull Request as you see fit.
Thanks!
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SET Evidence = "All 3 categories of PDE4 isoforms from all four subfamilies can interact with β-arrestin1/2,
implying that a common region in the PDE4 catalytic unit provides a
binding site for β-arrestins [65]. Thus challenge of cells with a β-agonist has
been shown to cause recruitment of a PDE4–arrestin complex to the β2- AR."
complex(p(SFAM:"PDE4 Family"),p(SFAM:"ARRB Family"))
act(p(HGNC:ADRB2)) directlyIncreases complex(p(HGNC:ADRB2),p(SFAM:"PDE4 Family"),p(SFAM:"ARRB Family"))
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