Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_assertion wasGeneratedBy ECO_0000203 NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_assertion wasDerivedFrom gad-20150221 NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_assertion SIO_000772 15148151 NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_assertion evidence source_evidence_literature NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.
- NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_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." NP85623.RAUIKrHJgQKpHmAd3OAcIa8cQvpgBei_PQabtVr4xB-z4130_provenance.