Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129663.RAeqYAtY2VxUCDa0vLlNjcfmmHq8mMaPgdxzBD1HT9dWs130_provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP64859.RA2jpTJ05GAdUktWumCJkAtgrHQUCPnT0R7bsrbAMa2Wo130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64859.RA2jpTJ05GAdUktWumCJkAtgrHQUCPnT0R7bsrbAMa2Wo130_provenance.
• NP64865.RAzBlwZbJMCpbcojvJGyvBbjqAxNH5tCUBHxpjV2mkwc8130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64865.RAzBlwZbJMCpbcojvJGyvBbjqAxNH5tCUBHxpjV2mkwc8130_provenance.
• NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125642.RAAA_pagyBfzKmz-38PcBDtM13hLIH0b5RPMNA_6QTHEw130_provenance.
• NP125652.RACn2I9rdzVFHvsyW9U0wQ1UR_Yc1R9exqh5ZSyP6Blak130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125652.RACn2I9rdzVFHvsyW9U0wQ1UR_Yc1R9exqh5ZSyP6Blak130_provenance.
• NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179952.RA0x1hNIn6SyqCCKLoONvBCLbZ--vWRpaACykKlD50fzE130_provenance.
• NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129664.RANn28j4B1wOcOD_jXLgNwJ8YFS6rnruuWCARHKV3ctek130_provenance.
• NP179951.RAZ12cwkK_eaXn34BvgPf47c2LbIgSNzAcNyUQjT-62D8130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179951.RAZ12cwkK_eaXn34BvgPf47c2LbIgSNzAcNyUQjT-62D8130_provenance.
• NP179955.RAX6SC3EvKWVluKB3A2_XU497FWBh9UfFtICOnyJeG8AI130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179955.RAX6SC3EvKWVluKB3A2_XU497FWBh9UfFtICOnyJeG8AI130_provenance.
• NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179957.RAeSiN4E3_mIW_xUuKCHjFMgf0BrTVgrbyS3lJdVQW-T4130_provenance.
• NP150053.RArfLNhnXcT8Dthxiv8ndO5toe71yhmof8hzZDoGjvdwI130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150053.RArfLNhnXcT8Dthxiv8ndO5toe71yhmof8hzZDoGjvdwI130_provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179956.RAIDHr8LSr4qqVaE4D6q013yA3aL1v0f011IcZRP3L_a8130_provenance.
• NP179953.RAsjGfXuqfXI1pgegLPeo4SRqtonJENBLQ-3QXv8PGoJU130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179953.RAsjGfXuqfXI1pgegLPeo4SRqtonJENBLQ-3QXv8PGoJU130_provenance.
• NP179954.RAtjVAIq8lL9dzDT7CKET6rWpmTME9KrWM_tASfcQpMX4130_assertion description "[This is the first description of an association of the SELP gene variant 168M with primary VF during acute MI. This variant may be a candidate polymorphism for evaluating the susceptibility for VF in the setting of acute MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179954.RAtjVAIq8lL9dzDT7CKET6rWpmTME9KrWM_tASfcQpMX4130_provenance.