Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_assertion description "[The chromosomal location for the spinocerebellar ataxia type 31 (SCA31) has been mapped to chromosome 16q22.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_assertion evidence source_evidence_literature NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_assertion SIO_000772 21267591 NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_assertion wasDerivedFrom befree-2016 NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_assertion wasGeneratedBy ECO_0000203 NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP867793.RAp-qcgYKcuoxBg_2DGlxSVhio_CTZXY7D4CUYr3eAgOE130_provenance.