Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion> ?p ?o ?g. }
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- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion type Assertion NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_head.
- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion description "[Aberrant methylation of the 11p15.5 imprinted region, through genetic or epigenetic mechanisms, leads to two clinical syndromes, with opposite growth phenotypes: Russell-Silver Syndrome (RSS; with severe fetal and postnatal growth retardation) and Beckwith-Wiedemann Syndrome (BWS; an overgrowth syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_provenance.
- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion evidence source_evidence_literature NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_provenance.
- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion SIO_000772 24322424 NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_provenance.
- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion wasDerivedFrom befree-2016 NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_provenance.
- NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_assertion wasGeneratedBy ECO_0000203 NP1135226.RAtzP9MYatJkVyx4dG0YuO08Nc3pM_DPISKchK_wKmI3s130_provenance.