Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_assertion wasGeneratedBy ECO_0000203 NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_assertion wasDerivedFrom befree-2016 NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_assertion SIO_000772 24092288 NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_assertion evidence source_evidence_literature NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.
- NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_assertion description "[Combined dystonias (with parkinsonism or myoclonus) are further subdivided into persistent (GCHI [DYT5], SGCE [DYT11], and ATP1A3 [DYT12], with TAF1 most likely but not yet proven to be linked to DYT3) and paroxysmal (PNKD [DYT8], PRRT2 [DYT10], and SLC2A1 [DYT18]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116032.RAyebU0vvqW-EAU5VOy6h9cSt_uLruHrv_1qKNdvIfyBM130_provenance.