Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP279082.RAbQTjgH3oixz2GQsbSINVWxO7K78Ay2c8Fr2S8T5vePg130_provenance.