Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion type Assertion NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_head.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion description "[These findings, combined with a Dock6 expression profile that is consistent with an AOS phenotype as well as the very recent demonstration of dominant mutations of ARHGAP31 in AOS, establish Cdc42 and Rac1 as key molecules in the pathogenesis of AOS and suggest that other regulators of these Rho GTPase proteins might be good candidates in the quest to define the genetic spectrum of this genetically heterogeneous condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_provenance.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion evidence source_evidence_literature NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_provenance.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion SIO_000772 21820096 NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_provenance.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion wasDerivedFrom befree-20140225 NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_provenance.
- NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_assertion wasGeneratedBy ECO_0000203 NP882693.RAeHAXtvP-QqywDIevuH2ZOfoqR0DSCmL64vPOY368-54130_provenance.