Matches in Nanopublications for { ?s ?p "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172299.RAgXlTYgaegOX8k8Wu8gMLQpAh6syla6bjre6dqkdKubc130_provenance.
- assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.