Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion> ?p ?o ?g. }
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- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion type Assertion NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_head.
- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion description "[Familial central diabetes insipidus is an inherited disease of predominant autosomal dominant trait characterized by a deficiency of arginine vasopressin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.
- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion evidence source_evidence_literature NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.
- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion SIO_000772 12012274 NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.
- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion wasDerivedFrom befree-20140225 NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.
- NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_assertion wasGeneratedBy ECO_0000203 NP681617.RA2Gi8jPzIVFGWGMQrMeKgSQPdiWhfNu_XOg64y-AYrDY130_provenance.