Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion> ?p ?o ?g. }
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- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion type Assertion NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_head.
- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion wasGeneratedBy ECO_0000203 NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_provenance.
- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion wasDerivedFrom befree-20140225 NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_provenance.
- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion SIO_000772 16615080 NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_provenance.
- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion evidence source_evidence_literature NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_provenance.
- NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_assertion description "[Novel studies establish that imprinting at one of these, the IGF2-H19 domain, is epigenetically deregulated (with loss of DNA methylation) in Silver-Russell Syndrome (SRS), a congenital disease of growth retardation and asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672666.RA6y8IrfYIeX2k9mCU8NevvmCxJi5cLrrnGyvnCzpsOQ8130_provenance.