Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion> ?p ?o ?g. }
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- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion type Assertion NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_head.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion evidence source_evidence_literature NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion SIO_000772 9302264 NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion wasDerivedFrom befree-2016 NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.
- NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_assertion wasGeneratedBy ECO_0000203 NP1380694.RADdrx00LRIWQ4W3L5uHfM6aOuvgEMvfDCFXalI2-16zc130_provenance.