Matches in Nanopublications for { ?s ?p "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4744.RAdAA09VEgnkoF8JResfuJra7P0lP9qPKzXPdb14Fo7bw130_provenance.
- assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936472.RAtOVya2w6t0vSZcYTgtXFQ3pFdtKGvCU-s5fisT2JFuI130_provenance.
- NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936476.RAOcQsa3ZcDBnT-mNuz--be2i4WLasChPUOh4u5_YxATo130_provenance.
- NP1086057.RAMUs51YJUBQDxJVDHk5BwhxMQP042bQOxxa2HxL1EWRw130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086057.RAMUs51YJUBQDxJVDHk5BwhxMQP042bQOxxa2HxL1EWRw130_provenance.
- NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086059.RAJ5vL1MPei1DVBJKmGMDGd5W1mwNKzg3NumKEe4LrXjA130_provenance.
- NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_assertion description "[Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7550.RA7GVQwq45QA0T12uNKCvQKGFQR8TpQo_ggLzjGTmY5ZA130_provenance.