Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_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." NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_assertion evidence source_evidence_literature NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_assertion SIO_000772 15389765 NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_assertion wasDerivedFrom befree-20140225 NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_assertion wasGeneratedBy ECO_0000203 NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807092.RAHwQ8jEeCaq1H9EYs4uMu8QTNA4YDxArPUYfKWLX5PMA130_provenance.