Matches in Nanopublications for { ?s ?p "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254156.RAdlv6bbIzLaQwO1i2QuV2KtwSDHkTUjhjZithROcLlRI130_provenance.
- NP758.RA3X0pO1VPB-KOZ1uIG6tj2l_LBknMJkabXQMmrVzrHMw130_assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758.RA3X0pO1VPB-KOZ1uIG6tj2l_LBknMJkabXQMmrVzrHMw130_provenance.
- NP703135.RAa5GmS__7uVCqrG2xWMWknGMQZRHi5FYeV0MHFpsCyvE130_assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703135.RAa5GmS__7uVCqrG2xWMWknGMQZRHi5FYeV0MHFpsCyvE130_provenance.
- NP5574.RAgzhraUQqjIKkRF2y0Wauei8jCYv2dw30IeUBD-eU1jM130_assertion description "[Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5574.RAgzhraUQqjIKkRF2y0Wauei8jCYv2dw30IeUBD-eU1jM130_provenance.