Matches in Nanopublications for { ?s ?p "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96314.RASfovHSiOBD_uH0VteArfMsMLqlY1mZQF8u04r9inTFQ130_provenance.
- NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66774.RApuPk6owoc0h9tWOYSKuzHW6z3dbC5PTXsNE6pX6a5bU130_provenance.
- assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP517080.RAGFqv954VG1TTOJT_wUgkPmGrsynBQ_PTOfOkHqWxqrM130_assertion description "[Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517080.RAGFqv954VG1TTOJT_wUgkPmGrsynBQ_PTOfOkHqWxqrM130_provenance.