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- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion type Assertion NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_head.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion description "[Hutchinson-Gilford Progeria Syndrome (HGPS) is a premature aging disorder caused by mutations in LMNA, which encodes the nuclear scaffold proteins lamin A and C. In HGPS and related progerias, processing of prelamin A is blocked at a critical step mediated by the zinc metalloprotease ZMPSTE24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion evidence source_evidence_literature NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion SIO_000772 23666920 NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion wasDerivedFrom befree-20140225 NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_assertion wasGeneratedBy ECO_0000203 NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.