Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP252460.RAs36T423X2AXEZtVeOmgX_sj8bKdTYlCzdlBg3QwzQZk130_provenance.