Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_assertion description "[Finally, paroxysmal exertion-induced dystonia (DYT18, GLUT1 deficiency) is caused by mutations in the SLC2A1 gene (DYT9 and DYT18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_assertion evidence source_evidence_literature NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_assertion SIO_000772 22166420 NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_assertion wasDerivedFrom befree-20150227 NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_assertion wasGeneratedBy ECO_0000203 NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP695643.RAHTBaLxWHFushW_hJlGQbM5vdAG7X85L1gJ49xbk6ak4130_provenance.