Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_assertion description "[Partial SPAST deletions, but not SPAST amplifications and SPG3A copy number aberrations, represent an underestimated cause of autosomal dominant hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_assertion evidence source_evidence_literature NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_assertion SIO_000772 17035675 NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_assertion wasDerivedFrom befree-20140225 NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_assertion wasGeneratedBy ECO_0000203 NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP349366.RAp-k4-hByUd5S5bxoEeQR7XLsuMirvwYhaNH055-LNEs130_provenance.