Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion> ?p ?o ?g. }
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- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion type Assertion NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_head.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion wasGeneratedBy ECO_0000203 NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion wasDerivedFrom befree-20150227 NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion SIO_000772 25038827 NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_assertion evidence source_evidence_literature NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.
- NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_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." NP880389.RAr8kWfjvjV6qmeWEOgAxB4kLwdMtEebVbvPGjONE1eBc130_provenance.