Matches in Nanopublications for { ?s ?p "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753269.RAe9phEY4sVhDPHQlbNaLV29gAnE1WSKCUUrsrXeYrLP8130_provenance.
- NP559131.RA3g75YoU1B15fM49mb-h9Up9nC3wBYQ4I85xAUV78km0130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559131.RA3g75YoU1B15fM49mb-h9Up9nC3wBYQ4I85xAUV78km0130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459169.RAOgGn2W3uMyVZ5GEEAQ0LM7iHbwAUdCpNE5JYiNZgKKg130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459169.RAOgGn2W3uMyVZ5GEEAQ0LM7iHbwAUdCpNE5JYiNZgKKg130_provenance.