Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_assertion description "[Identification of SCA2 mutation in cases of spinocerebellar ataxia with no family history in mid-eastern Sicily.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_assertion evidence source_evidence_literature NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_assertion SIO_000772 10551907 NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_assertion wasDerivedFrom befree-2016 NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_assertion wasGeneratedBy ECO_0000203 NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.
- befree-2016 importedOn "2016-02-19" NP267130.RA_S7Oi0S6ThGWdQ_le5IuPrnY1d0Doenz_k7txzn8lQw130_provenance.