Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP477596.RAVGEZ3I18-35SpWbNrAzJSsJb1y579WhwZ-K003H26QU130_provenance.