Matches in Nanopublications for { ?s ?p "[40% of all mutations identified among the Polish acute intermittent porphyria (AIP) patients in this study are novel, indicating the heterogeneity of molecular defects causing AIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[40% of all mutations identified among the Polish acute intermittent porphyria (AIP) patients in this study are novel, indicating the heterogeneity of molecular defects causing AIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_assertion description "[40% of all mutations identified among the Polish acute intermittent porphyria (AIP) patients in this study are novel, indicating the heterogeneity of molecular defects causing AIP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193379.RAescKFwStty2fHplpkBH8-uCPU04DFK5osXWYEG2RoGA130_provenance.