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- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_assertion type Assertion NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_head.
- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_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." NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_provenance.
- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_assertion evidence source_evidence_literature NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_provenance.
- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_assertion SIO_000772 22272310 NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_provenance.
- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_assertion wasDerivedFrom befree-2016 NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_provenance.
- NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_assertion wasGeneratedBy ECO_0000203 NP955654.RA8AH4Aneh-X_rrjxt41xHnUkKQJEBNXlERaEn3QDbWcw130_provenance.