Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion> ?p ?o ?g. }
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- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion type Assertion NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_head.
- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion description "[We have shown previously that the ubiquitin ligase MID1, mutations of which cause the midline malformation Opitz BBB/G syndrome (OS), serves as scaffold for a microtubule-associated protein complex that regulates protein phosphatase 2A (PP2A) activity in a ubiquitin-dependent manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_provenance.
- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion evidence source_evidence_literature NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_provenance.
- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion SIO_000772 21930711 NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_provenance.
- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion wasDerivedFrom befree-2016 NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_provenance.
- NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_assertion wasGeneratedBy ECO_0000203 NP924784.RAhl9nRNUSIG4uYju9BqMQx4Q_rkdoyaf6qDRFwZ5utm0130_provenance.