Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_assertion description "[DYT1 primary torsion dystonia is an autosomal dominant movement disorder due to a 3-bp GAG deletion in the TOR1A gene, which becomes manifest in only 30-40% of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_assertion evidence source_evidence_literature NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_assertion SIO_000772 17105745 NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_assertion wasDerivedFrom befree-2016 NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_assertion wasGeneratedBy ECO_0000203 NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.
- befree-2016 importedOn "2016-02-19" NP579349.RAvV8ao9wAFa9HpgPynfRXoGCTM-IzR_r7UzE1Yu1rkJo130_provenance.