Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_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." NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_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.
- NP877390.RAKMvwXEJI2pPD5hs8DTM1nVpxmmtempSVvV3nXHZLLOk130_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." NP877390.RAKMvwXEJI2pPD5hs8DTM1nVpxmmtempSVvV3nXHZLLOk130_provenance.
- NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_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." NP483842.RA6HlGYkaGRwIA1A9TVARhCZ6-B6Os-KRTsMVSafludlg130_provenance.
- NP544992.RA4Ma8Qk77ed7nHJzqpPVsTcSD4fZ9DQFS_aBsbPeMi0E130_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." NP544992.RA4Ma8Qk77ed7nHJzqpPVsTcSD4fZ9DQFS_aBsbPeMi0E130_provenance.
- 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." provenance.