Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_assertion description "[SLC30A6 has been implicated in Alzheimer disease, so these fusion gene data could explain a report of spastic paraplegia and dementia cosegregating in a family with deletion of the final exon of SPAST.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_assertion evidence source_evidence_literature NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_assertion SIO_000772 25065914 NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_assertion wasDerivedFrom befree-2016 NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_assertion wasGeneratedBy ECO_0000203 NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1205347.RAvGH87FnMVeLtqvw3n5thDnzklMVfBYrwCtPZw8OkOVc130_provenance.