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- source_evidence_literature type ECO_0000212 NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP839986.RAmHvZfz6sPhruR-yKVib3G3U694Pc_GfVrvisfXG9xtI130_provenance.