Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion type Assertion NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_head.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion description "[The triple A syndrome (MIM#231550) is a rare autosomal recessive disorder characterized by adrenocorticotropic hormone (ACTH) resistant adrenal failure, achalasia, alacrima, and a variety of neurological and dermatological features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_provenance.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion evidence source_evidence_literature NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_provenance.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion SIO_000772 15666842 NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_provenance.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion wasDerivedFrom befree-2016 NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_provenance.
- NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_assertion wasGeneratedBy ECO_0000203 NP477597.RAljKFR33Rd--t972QSn3c6Jj3eX0M0v14tRc2W1oGy4M130_provenance.