Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_assertion wasGeneratedBy ECO_0000203 NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_assertion wasDerivedFrom befree-2016 NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_assertion SIO_000772 25038827 NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_assertion evidence source_evidence_literature NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.
- NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_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." NP1202879.RAAsEO-FGqJ6JGBJp0nvEUJIcjiyUE50J9YScTToUUa1U130_provenance.