Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion> ?p ?o ?g. }
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- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion type Assertion NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_head.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_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." NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion evidence source_evidence_literature NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion SIO_000772 23666920 NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion wasDerivedFrom befree-20150227 NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_assertion wasGeneratedBy ECO_0000203 NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.