Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion> ?p ?o ?g. }
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- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion type Assertion NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_head.
- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion description "[Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) has been known as a rare disorder transmitted as an autosomal dominant trait, characterized by polyuria and polydipsia, and caused by deficient neurosecretion of arginine vasopressin precursor (AVP-NPII).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion evidence source_evidence_literature NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion SIO_000772 15811933 NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion wasDerivedFrom befree-20140225 NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_assertion wasGeneratedBy ECO_0000203 NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.