Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_assertion wasGeneratedBy ECO_0000203 NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_assertion wasDerivedFrom befree-20150227 NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_assertion SIO_000772 15148151 NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_assertion evidence source_evidence_literature NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.
- NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_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." NP681481.RArCAZ-cb53zPGWa9aKjW0A92VvP1iMHEJ_Z1x4C8AlKU130_provenance.