Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- gad-20150221 importedOn "2015-02-21" NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_assertion wasGeneratedBy ECO_0000203 NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_assertion wasDerivedFrom gad-20150221 NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_assertion SIO_000772 15148151 NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_assertion evidence source_evidence_literature NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.
- NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_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." NP52202.RAtTwDflE7QOZ-Ty879y3iBWyKsa4LsqVfcwhjfaQ_22o130_provenance.