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- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_assertion type Assertion NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_head.
- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_assertion wasGeneratedBy ECO_0000203 NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_provenance.
- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_assertion wasDerivedFrom befree-20150227 NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_provenance.
- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_assertion SIO_000772 23335487 NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_provenance.
- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_assertion evidence source_evidence_literature NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_provenance.
- NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_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." NP705687.RAo7-DFH0cq9_kae30u9Ru9WU8DBmVBJMpboKHLGz6KxI130_provenance.