Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion> ?p ?o ?g. }
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- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion type Assertion NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_head.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion wasGeneratedBy ECO_0000203 NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion wasDerivedFrom befree-2016 NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion SIO_000772 25038827 NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_assertion evidence source_evidence_literature NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.
- NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_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." NP1202878.RA8vOTx0by8z_DGLzTaTfMYPuPXnXjs97I1ET8OMZU5To130_provenance.