Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_assertion wasGeneratedBy ECO_0000203 NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_assertion wasDerivedFrom gad-20130706 NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_assertion SIO_000772 15148151 NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_assertion evidence source_evidence_literature NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia SCA 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 FGF14-SCA, and dentatorubral-pallidoluysian atrophy DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.
- gad-20130706 importedOn "2013-07-06" NP62329.RAKDLPCoZH9eFMjD9IWrVQHb-UUGnmzVfwXaSLMMWAVhQ130_provenance.