Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion> ?p ?o ?g. }
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- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion type Assertion NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_head.
- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion description "[Mutations in AQP2 cause autosomal nephrogenic diabetes insipidus (NDI), a disease that renders the kidney unresponsive to vasopressin, resulting in polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_provenance.
- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion evidence source_evidence_literature NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_provenance.
- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion SIO_000772 19701945 NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_provenance.
- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion wasDerivedFrom befree-20150227 NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_provenance.
- NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_assertion wasGeneratedBy ECO_0000203 NP249343.RAPG1C7oEpdW0Vc8qmzt_dm2ftQCjcD1EiNB_OkXnvRJ0130_provenance.