Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion> ?p ?o ?g. }
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- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion type Assertion NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_head.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion description "[Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion evidence source_evidence_literature NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion SIO_000772 20384727 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion wasDerivedFrom befree-2016 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.
- NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_assertion wasGeneratedBy ECO_0000203 NP805588.RA1-Z7rcGgI5gCXiW9sRYUoIN6lOpeWnuZW2LYxHqNEx4130_provenance.