Matches in Nanopublications for { ?s ?p "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121293.RAXqKQDSlCq0sgK51oDM-fKhOTA--vKINixHoEeFQ3w9w130_provenance.
- assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP184644.RAU0Qzj7t2zgZZb_ZGYTUfjoKzycu3Al0aXc-A9Ej8oP8130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184644.RAU0Qzj7t2zgZZb_ZGYTUfjoKzycu3Al0aXc-A9Ej8oP8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP67944.RAlxyaYR3iot7PBdz1-K4OlkZr_CAjOSsSoE1aCaISgq8130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67944.RAlxyaYR3iot7PBdz1-K4OlkZr_CAjOSsSoE1aCaISgq8130_provenance.
- NP90997.RA9IC-rP9KqUZSSKvE-nGK9hvghV89I2owEOtn9FJsLfc130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90997.RA9IC-rP9KqUZSSKvE-nGK9hvghV89I2owEOtn9FJsLfc130_provenance.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.
- NP184647.RAEJB3MuVPffnw5Fmd69avngRLiYpVqqeEPoz8C8YyFAQ130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184647.RAEJB3MuVPffnw5Fmd69avngRLiYpVqqeEPoz8C8YyFAQ130_provenance.
- NP184646.RAz93DUCFpSDzeyWyNUJQA_0sxAVKAsDed9ltPDqZAEAY130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184646.RAz93DUCFpSDzeyWyNUJQA_0sxAVKAsDed9ltPDqZAEAY130_provenance.