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- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_assertion type Assertion NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_head.
- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_assertion wasGeneratedBy ECO_0000203 NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_provenance.
- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_assertion wasDerivedFrom befree-20140225 NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_provenance.
- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_assertion SIO_000772 16615080 NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_provenance.
- NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_assertion evidence source_evidence_literature NP450587.RAT1e-iW14mGfQN3TEjBskOWz_Wb0LUiVrHdryBvM2Fyw130_provenance.
- 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.