Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion> ?p ?o ?g. }
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- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion type Assertion NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_head.
- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion wasGeneratedBy ECO_0000203 NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_provenance.
- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion wasDerivedFrom befree-2016 NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_provenance.
- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion SIO_000772 23462481 NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_provenance.
- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_assertion evidence source_evidence_literature NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_provenance.
- NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_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." NP1057965.RANsVsXG03VdAd3JwZ7vNPlDZtMeHSSZY_zeCnyU8Cvqc130_provenance.