Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_assertion description "[Peroneal muscular atrophy (PMA) associated with hereditary spastic paraparesis (HSP) is a nosologically ill-defined disease, which has been classified by Dyck as hereditary motor and sensory neuropathy type V (HMSN V).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_assertion evidence source_evidence_literature NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_assertion SIO_000772 1557949 NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_assertion wasDerivedFrom befree-20140225 NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_assertion wasGeneratedBy ECO_0000203 NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP763327.RAvbTHUFl5A79C6SvGSHAwaDUR6u16-HxBlDrh9Zv6W7k130_provenance.