Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion description "[Spinocerebellar ataxia type 17 (SCA17) is an autosomal dominant cerebellar ataxia caused by expansion of CAG/CAA trinucleotide repeats in the TATA-binding protein (TBP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion evidence source_evidence_literature NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion SIO_000772 14967767 NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion wasDerivedFrom befree-2016 NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_assertion wasGeneratedBy ECO_0000203 NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.
- befree-2016 importedOn "2016-02-19" NP431999.RApwPixxUrsLyFznf1sczgn91AKU7ie4QN_fDXQFuiLis130_provenance.