Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_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." NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_assertion evidence source_evidence_literature NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_assertion SIO_000772 16120822 NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_assertion wasDerivedFrom befree-2016 NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_assertion wasGeneratedBy ECO_0000203 NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.
- befree-2016 importedOn "2016-02-19" NP510472.RAbYciT4mUhbVIsjlLZxZbDrQwxHGLrrAa7aVViOUFrxA130_provenance.