Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion> ?p ?o ?g. }
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- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion type Assertion NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_head.
- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion wasGeneratedBy ECO_0000218 NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_provenance.
- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion wasDerivedFrom uniprot-20130724 NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_provenance.
- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion SIO_000772 21376300 NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_provenance.
- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion evidence source_evidence_curated NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_provenance.
- NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_assertion description "[Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2919.RAyh-Y0nKNndwF6ilJo2CSiU853N4zU-nOCWY0kZn8fvc130_provenance.