Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion> ?p ?o ?g. }
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- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion type Assertion NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_head.
- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_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." NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion evidence source_evidence_literature NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion SIO_000772 15666842 NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion wasDerivedFrom befree-20140225 NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_assertion wasGeneratedBy ECO_0000203 NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.