Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion> ?p ?o ?g. }
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- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion type Assertion NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_head.
- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion wasGeneratedBy ECO_0000203 NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_provenance.
- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion wasDerivedFrom befree-20150227 NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_provenance.
- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion SIO_000772 21863054 NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_provenance.
- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion evidence source_evidence_literature NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_provenance.
- NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_assertion description "[DNA methylation defects involving ICR1 result in two growth disorders with opposite phenotypes: an overgrowth disorder, the Beckwith-Wiedemann syndrome (maternal ICR1 hypermethylation in 10% of BWS cases) and a growth retardation disorder, the Silver-Russell syndrome (paternal ICR1 loss of methylation in 60% of SRS cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303986.RAD4yjOOJkRcWNSwitLY56h-_oIP9zIFzYbEq9pwrn7K8130_provenance.