. . . . . . . "[Homozygous absence of SMN1 exons 7 and 8, or exon 7 only, was found in 80% of childhood spinal muscular atrophy patients/those patients, 45% were also deleted for NAIP exon 5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:16:19+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .