Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_assertion description "[Here, we report on the screening of the whole coding sequence of the ABCR gene in 40 unrelated STGD and 15 FFM families and we show that mutations truncating the ABCR protein consistently led to STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_assertion evidence source_evidence_literature NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_assertion SIO_000772 9781034 NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_assertion wasDerivedFrom befree-20140225 NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_assertion wasGeneratedBy ECO_0000203 NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.
- befree-20140225 importedOn "2014-02-25" NP301538.RAn6B9MY1kqG_0395P54G-Sou6dY0UEZh_cty7DB-Z9ys130_provenance.