Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion> ?p ?o ?g. }
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- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion type Assertion NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_head.
- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion wasGeneratedBy ECO_0000203 NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_provenance.
- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion wasDerivedFrom befree-2016 NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_provenance.
- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion SIO_000772 23462481 NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_provenance.
- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion evidence source_evidence_literature NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_provenance.
- NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_assertion description "[Changes in a long list of additional genes have been suggested as causes for parkinsonism or PD, including genes for hereditary ataxias (ATXN2, ATXN3, FMR1), frontotemporal dementia (C9ORF72, GRN, MAPT, TARDBP), DYT5 (GCH1, TH, SPR), and others (ATP13A2, CSF1R, DNAJC6, FBXO, GIGYF2, HTRA2, PLA2G6, POLG, SPG11, UCHL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057967.RA2_1vfM5mbwclUGDQi2Ca7M3LYqxluBvPBFN5uMbvDoA130_provenance.