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- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_assertion type Assertion NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_head.
- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_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." NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_assertion evidence source_evidence_literature NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_assertion SIO_000772 15666842 NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_assertion wasDerivedFrom befree-2016 NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_assertion wasGeneratedBy ECO_0000203 NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.