. . . . . . . "[In contrast to lethal neonatal RDS resulting from homozygous or compound heterozygous ABCA3 mutations, single ABCA3 mutations are overrepresented among European-descent infants ?34 weeks' gestation with RDS and account for ~10.9% of the attributable risk among term and late preterm infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:10:12+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .