Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion> ?p ?o ?g. }
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- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion type Assertion NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_head.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion description "[Mutations in SLC6A5, encoding GlyT2, cause hereditary hyperekplexia in humans, and similar phenotypes in knock-out mice, and variants are associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion evidence source_evidence_literature NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion SIO_000772 22272310 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion wasDerivedFrom befree-20140225 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion wasGeneratedBy ECO_0000203 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.