Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_assertion description "[However, at least half of dominant ataxias (SCAs) are caused by (CAG)n repeat expansions resulting in expanded polyglutamine tracts (SCAs 1, 2, 3, 6, 7, 17, and DRPLA), although of the remainder only SCAs 8, 10, 12, 14, 15/16, and 31 are frequent enough that the described phenotype is probably representative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_assertion evidence source_evidence_literature NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_assertion SIO_000772 25192506 NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_assertion wasDerivedFrom befree-2016 NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_assertion wasGeneratedBy ECO_0000203 NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217268.RApf1StHLSuV56XmFPVcg1ydAU0maEh9omeX8NpM8jz3w130_provenance.