Matches in Nanopublications for { ?s ?p "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1307585.RAjlDLJy1EnuBIi_qDLZrblI6EOrP1zaRURv-VPknNzCA130_assertion description "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307585.RAjlDLJy1EnuBIi_qDLZrblI6EOrP1zaRURv-VPknNzCA130_provenance.
- NP1307586.RALUhf5PBiuItis9taLco2M3wVGXXDqOM7EFlcfWXrGTM130_assertion description "[The most frequent cause for an abnormal result during screening of newborn infants for galactosemia is double heterozygosity for Duarte variant and galactosemia, in which galactose-1-phosphate uridyl transferase activity is reduced to approximately 17% of normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307586.RALUhf5PBiuItis9taLco2M3wVGXXDqOM7EFlcfWXrGTM130_provenance.