Matches in Nanopublications for { ?s ?p "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP607202.RAWIZiFwyiyP11iZ5S1fj0nfWKYRCW22HmwanXQIDV0Fw130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607202.RAWIZiFwyiyP11iZ5S1fj0nfWKYRCW22HmwanXQIDV0Fw130_provenance.
- NP607203.RAbRUfyIhrF-KptEWa24NSfgK15DoigtkpqoPPc0mIi-I130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607203.RAbRUfyIhrF-KptEWa24NSfgK15DoigtkpqoPPc0mIi-I130_provenance.
- NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522224.RAPvh1Il6CAEzA1cFQK3_abSSWxl6UDxjb_UsEVZ9j__0130_provenance.
- NP523300.RAKzoPGQqKbhcrUNQS_allWa7JoV8isyQ5pZP-1iM_UXo130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523300.RAKzoPGQqKbhcrUNQS_allWa7JoV8isyQ5pZP-1iM_UXo130_provenance.