Matches in Nanopublications for { ?s ?p "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi_yPLpg130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69223.RAZzDTIJTy2m8WmIGSxqP8Vn8M2tREgrCqz3CBi_yPLpg130_provenance.
- NP76915.RAcjNlE3-ZZhw_3gpBC15z9A-irlT-4kaHDXEZsRu_zdc130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76915.RAcjNlE3-ZZhw_3gpBC15z9A-irlT-4kaHDXEZsRu_zdc130_provenance.
- NP77550.RAc5MANgr4SLozw_nhYF7k9Ch-U6LsT_SZnCgHjzzk1qI130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77550.RAc5MANgr4SLozw_nhYF7k9Ch-U6LsT_SZnCgHjzzk1qI130_provenance.
- NP249914.RASHlmqEa9rJGKstp1unkNBfGfaxIv9Ye0hH_gVG7Odag130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249914.RASHlmqEa9rJGKstp1unkNBfGfaxIv9Ye0hH_gVG7Odag130_provenance.
- NP253803.RA7Y3vyfMT3QTHfKApmd61XZ3DX3kbkkHBkZsAvlICdtU130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253803.RA7Y3vyfMT3QTHfKApmd61XZ3DX3kbkkHBkZsAvlICdtU130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228595.RAei9S2_kFs7UJ2WiN3a1-uK-QVxlHGaEpGGTFFIfyOJk130_provenance.
- NP80342.RAUS9eAs-LHZ4puJkkOULQgIqLMmPtZjOvIe0T6Vb_oRI130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP80342.RAUS9eAs-LHZ4puJkkOULQgIqLMmPtZjOvIe0T6Vb_oRI130_provenance.
- NP81027.RALqyOyz2O2ivYsZsg79s6b12xsJSmNefKie5IY1BYK9o130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81027.RALqyOyz2O2ivYsZsg79s6b12xsJSmNefKie5IY1BYK9o130_provenance.
- NP919668.RAj9TYSXgW7DS9kXcfwQL5zCePsnq_hLNElDP57F_RzxE130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919668.RAj9TYSXgW7DS9kXcfwQL5zCePsnq_hLNElDP57F_RzxE130_provenance.
- NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP113104.RARMTJxOo72wGlkEJVlqbWUpNntcZNCO4S6tPoZtwCAJc130_provenance.
- NP581585.RAMpXl7OqOpDvxQQT4oy9MyFJuHQF7v2nwx8bwsXujPtQ130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581585.RAMpXl7OqOpDvxQQT4oy9MyFJuHQF7v2nwx8bwsXujPtQ130_provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP146503.RAfZVjg0I0cerjkmRgdYDheiy3NeqI-7RH2TOXb4O8Nb8130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146503.RAfZVjg0I0cerjkmRgdYDheiy3NeqI-7RH2TOXb4O8Nb8130_provenance.
- NP90938.RAtehiClhiRyA9nTZ1hVbT8CIOkJozYnMeRg1QtMAwhVg130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90938.RAtehiClhiRyA9nTZ1hVbT8CIOkJozYnMeRg1QtMAwhVg130_provenance.
- NP123394.RAllfYF-C6z-SS0s0vtOUPdlMvvHcv1lJViDHdr_u8bys130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123394.RAllfYF-C6z-SS0s0vtOUPdlMvvHcv1lJViDHdr_u8bys130_provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146499.RAmF8FsP62zOavmL9ArcAC2DMw47FNJEWZ_-nOSOAUFRM130_provenance.
- NP146500.RAl4_m22UtSHWQIIbeZgAGwQrhsYgsZdb76Dsl9UB_vYA130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146500.RAl4_m22UtSHWQIIbeZgAGwQrhsYgsZdb76Dsl9UB_vYA130_provenance.
- NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP114572.RA_-XxlPLX5MwEy5o4fZttxrs9fHwhU-XkSi-mhll60DM130_provenance.
- NP121300.RA6Dz_mMmWLTWMjBBXZ6fQK-NL145lVremfKJZMHKyUYs130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121300.RA6Dz_mMmWLTWMjBBXZ6fQK-NL145lVremfKJZMHKyUYs130_provenance.
- NP125656.RA5qKXJqgWFO88KIbZAzk2QYmnw203Qhv1rHfcb_0-hoY130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125656.RA5qKXJqgWFO88KIbZAzk2QYmnw203Qhv1rHfcb_0-hoY130_provenance.
- NP146501.RAz4fl0i-ATU9A3alj4InpXo_Yd_BpebhHQYeOylWByys130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146501.RAz4fl0i-ATU9A3alj4InpXo_Yd_BpebhHQYeOylWByys130_provenance.
- NP146502.RA4MqYF77JxxmVqisYNB3jhR7bratn8pgkb2p3qyKiA-M130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146502.RA4MqYF77JxxmVqisYNB3jhR7bratn8pgkb2p3qyKiA-M130_provenance.
- NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146504.RA8jrQZxBTeeF5cwkT3veCzwwt7Jih9tAA0VhVcUs9CNk130_provenance.