Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion> ?p ?o ?g. }
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- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion type Assertion NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_head.
- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion wasGeneratedBy ECO_0000203 NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_provenance.
- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion wasDerivedFrom befree-20150227 NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_provenance.
- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion SIO_000772 23335487 NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_provenance.
- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion evidence source_evidence_literature NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_provenance.
- NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_assertion description "[Our data reveal a broad range of epimutations exist in certain imprinting syndromes, with the exception of Prader-Willi syndrome and Angelman syndrome patients that are associated with solitary SNRPN-DMR defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705640.RAxSmG6dg58E8bB5nlu8Aag6wKzCb4Tntay9mseWTOZHk130_provenance.