Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion> ?p ?o ?g. }
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- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion type Assertion NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_head.
- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_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." NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_provenance.
- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion evidence source_evidence_literature NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_provenance.
- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion SIO_000772 15389765 NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_provenance.
- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion wasDerivedFrom gad-20150221 NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_provenance.
- NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_assertion wasGeneratedBy ECO_0000203 NP73049.RAKsnOmopeVYwmHDnbbBwY0t220zoXm1f2tFUdzyl0jgU130_provenance.