Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion> ?p ?o ?g. }
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- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion type Assertion NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_head.
- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_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." NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_provenance.
- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion evidence source_evidence_literature NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_provenance.
- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion SIO_000772 15389765 NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_provenance.
- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion wasDerivedFrom befree-20140225 NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_provenance.
- NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_assertion wasGeneratedBy ECO_0000203 NP896479.RA3WxN_5V4q6rTDWVnVoC_WCFn7K0K03waXelikGe2mwI130_provenance.