Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_assertion> ?p ?o ?g. }
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- NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_assertion type Assertion NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_head.
- NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_assertion description "[epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_provenance.
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- NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_assertion wasDerivedFrom lhgdn-20090331 NP216035.RAclyorcrUdUWJ7dcvlO7eBeeX9ss6Q7bDd-uYZpHIWDA130_provenance.
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