Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_assertion description "[Screening of 49 patients suffering from BPAD, 78 patients with SZ and 62 control individuals revealed eleven sequence variations including a 3 bp deletion within the 5'UTR (5' untranslated region), four exonic and five intronic SNPs as well as a point mutation in the 3'UTR of HTR3B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_assertion evidence source_evidence_literature NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_assertion SIO_000772 15389765 NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_assertion wasDerivedFrom befree-2016 NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_assertion wasGeneratedBy ECO_0000203 NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.
- befree-2016 importedOn "2016-02-19" NP461619.RAByBGTkNxDYkA2mxlE-r1QZZf6KXhC4Xz3AsCGDnUFuk130_provenance.