Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP695503.RAU2xQEZj-arQnH6XTEeLrbCLR27EJb7d2C3jVZEAC-EU130_provenance.