Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion> ?p ?o ?g. }
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- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion type Assertion NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_head.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion wasGeneratedBy ECO_0000203 NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion wasDerivedFrom befree-20140225 NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion SIO_000772 8664297 NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion evidence source_evidence_literature NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.
- NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_assertion description "[Using cloned fragments from the myotonic dystrophy (DM) and fragile X syndrome (FRAXA) loci containing normal, premutation, and full mutation lengths of repeats, we report the formation of novel alternative DNA secondary structures that map within the repeat tracts during reannealing of complementary strands, containing equal lengths of repeats, into linear duplex DNA molecules.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776966.RAtT8FrEabIWyFeGA-dSK5uUDKUtLZRqnctLL1dDF0Fbg130_provenance.