Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_assertion description "[Three additional autosomal dominant forms (DYT9, DYT19 and DYT20) might exist based on linkage mapping to regions apparently different from, yet in close proximity to or overlapping with the known loci DYT18, DYT10 and DYT8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_assertion evidence source_evidence_literature NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_assertion SIO_000772 19578124 NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_assertion wasDerivedFrom befree-20140225 NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_assertion wasGeneratedBy ECO_0000203 NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP612107.RAAWNWfBVwKOahUgWXeMDr374ROLdHZPGoKX8cFmqFA9U130_provenance.