Matches in Nanopublications for { ?s ?p "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251049.RAXfn9Zm2-To63bV6YrDoXtKVsN0-AP2MHJB2CoFvDiJY130_provenance.
- assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577277.RABTdi9EQkG5nXY71-EQ0-d7kIAxHwp0s3k2O6602CYhE130_provenance.
- NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_assertion description "[Mutations in the MTR gene, which encodes methionine synthase on human chromosome 1p43, result in the methylcobalamin deficiency G (cblG) disorder, which is characterized by homocystinuria, hyperhomocysteinemia, and hypomethioninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358021.RA1IJw6hE0z8qh8UAkt--XSotGU5xkdes5Y3kx6qfUM4E130_provenance.