Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_assertion description "[These novel mutations have also resulted in osteopenia, bilateral sensorineural deafness and pancreatic exocrine insufficiency, features that have not previously been associated with GLIS3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_assertion evidence source_evidence_literature NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_assertion SIO_000772 21139041 NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_assertion wasDerivedFrom befree-2016 NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_assertion wasGeneratedBy ECO_0000203 NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.
- befree-2016 importedOn "2016-02-19" NP857496.RAnxXEuT0iP8zbFLfkVgpdI1Ya_SkxvXRYImaZcIxoizY130_provenance.