Matches in Nanopublications for { ?s ?p "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP399639.RADLkJKzQUKDqF8fLGZm9HPxQc-__ERfgLFNpvXu3tNnk130_assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399639.RADLkJKzQUKDqF8fLGZm9HPxQc-__ERfgLFNpvXu3tNnk130_provenance.
- assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP1086056.RAHtQOthRrHq30DdhDxROZqowOe9dIyaF376WBtatrjTo130_assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086056.RAHtQOthRrHq30DdhDxROZqowOe9dIyaF376WBtatrjTo130_provenance.