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- source_evidence_literature type ECO_0000212 NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_assertion description "[These data indicate that dominant NDI in this family is due to a R254L mutation, resulting in the loss of arginine vasopressin-mediated phosphorylation of AQP2 at S256, and illustrates the in vivo importance of phosphorylation of AQP2 at S256 for the first time.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_assertion evidence source_evidence_literature NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_assertion SIO_000772 16120822 NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_assertion wasDerivedFrom befree-2016 NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_assertion wasGeneratedBy ECO_0000203 NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.
- befree-2016 importedOn "2016-02-19" NP510470.RAvdPRYH8xjBes9znAl6JxpEZ2jHmo7WqOgGQYbTn2h9g130_provenance.