Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion> ?p ?o ?g. }
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- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion type Assertion NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_head.
- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_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." NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_provenance.
- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion evidence source_evidence_literature NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_provenance.
- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion SIO_000772 15666842 NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_provenance.
- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion wasDerivedFrom befree-20140225 NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_provenance.
- NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_assertion wasGeneratedBy ECO_0000203 NP302442.RAlmxORVfX8E8M6hi73yfxYN1i0Ut2cORX7lg3IUivka4130_provenance.