Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion> ?p ?o ?g. }
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- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion type Assertion NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_head.
- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion description "[This report delineates the phenotypic features in a cohort of 58 individuals with Smith-Magenis syndrome (SMS) and compares features of patients with the common microdeletion to those of patients with variable sized deletions, and the three previously reported patients who harbor a mutation in RAI1 (retinoic acid induced 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_provenance.
- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion evidence source_evidence_literature NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_provenance.
- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion SIO_000772 14614393 NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_provenance.
- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion wasDerivedFrom befree-20140225 NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_provenance.
- NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_assertion wasGeneratedBy ECO_0000203 NP198652.RAtMfFrp527HXFWlRHvaojzZ00IpXaMH0mKaRvsmwOb5w130_provenance.