Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant cerebellar ataxia associated with small expansions of the trinucleotide repeat (CAG)n in the gene CACNL1A4 on chromosome 19p13, which encodes the alpha1 subunit of a P/Q-type voltage-gated calcium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_assertion evidence source_evidence_literature NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_assertion SIO_000772 9403487 NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_assertion wasDerivedFrom befree-20140225 NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_assertion wasGeneratedBy ECO_0000203 NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP440971.RA6Kqodketj_fJ1PGee5QMkJ6g5lgw-l9I9x_XnfBK6bw130_provenance.