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- source_evidence_literature type ECO_0000212 NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_assertion description "[The region mutated in Liddle syndrome, called the PY motif (L/PPxY), serves as a binding site for the ubiquitin ligase Nedd4-2, a C2-WW-Hect E3 ubiquitin ligase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_assertion evidence source_evidence_literature NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_assertion SIO_000772 18691017 NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_assertion wasDerivedFrom befree-2016 NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_assertion wasGeneratedBy ECO_0000203 NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.
- befree-2016 importedOn "2016-02-19" NP686848.RAnXpm9Ss8oDaPEiO6omjnsecmeBzrRWgJHcCUN9iL_SM130_provenance.