Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion> ?p ?o ?g. }
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- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion type Assertion NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_head.
- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion description "[The SCA2 mutation causes the disease in nearly 14% of autosomal dominant SCA in Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion evidence source_evidence_literature NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion SIO_000772 10735276 NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion wasDerivedFrom befree-2016 NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_assertion wasGeneratedBy ECO_0000203 NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.