Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion> ?p ?o ?g. }
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- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion type Assertion NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_head.
- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_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." NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_provenance.
- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion evidence source_evidence_literature NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_provenance.
- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion SIO_000772 22272310 NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_provenance.
- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion wasDerivedFrom befree-20150227 NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_provenance.
- NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_assertion wasGeneratedBy ECO_0000203 NP698017.RAVnKWkA8-WKptgqJWcnoWM16fKGZ8G9cGGSzgLZKd3o8130_provenance.