Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion> ?p ?o ?g. }
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- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion type Assertion NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_head.
- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_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." NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_provenance.
- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion evidence source_evidence_literature NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_provenance.
- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion SIO_000772 22272310 NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_provenance.
- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion wasDerivedFrom befree-20150227 NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_provenance.
- NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_assertion wasGeneratedBy ECO_0000203 NP423669.RAPQG67i707TXlktRgoZ7e999xX_SPYEXNmRJGQcZXq_Q130_provenance.