Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion type Assertion NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_head.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion wasGeneratedBy ECO_0000203 NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion wasDerivedFrom befree-20150227 NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion SIO_000772 25038827 NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion evidence source_evidence_literature NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.
- NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_assertion description "[By enzymatically characterizing Aicardi-Goutières syndrome (AGS)-associated SAMHD1 mutations and mutations in the allosteric dGTP-binding site of SAMHD1 for defects in RNase or dNTPase activity, we identify SAMHD1 point mutants that cause loss of one or both functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880399.RAeZwu0Ske161R24ETjpYXW7vJqJRyrPPRC_GoMe141jc130_provenance.