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- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion type Assertion NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_head.
- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion description "[A heterozygous G-to-A mutation at position 3823 (D1275N) in a highly conserved residue of exon 21 is associated with an autosomal dominant cardiac conduction disorder, sinus node dysfunction, arrhythmia, ventricular dilatation & dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_provenance.
- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion evidence source_evidence_literature NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_provenance.
- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion SIO_000772 15466643 NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_provenance.
- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion wasDerivedFrom lhgdn-20090331 NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_provenance.
- NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_assertion wasGeneratedBy ECO_0000203 NP206869.RAFHtEhdVtg7ShOYe7-kyD1BNuznquSZBC5Qwjlb1t0OY130_provenance.