Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion> ?p ?o ?g. }
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- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion type Assertion NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_head.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_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." NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion evidence source_evidence_literature NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion SIO_000772 23666920 NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion wasDerivedFrom befree-2016 NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.
- NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_assertion wasGeneratedBy ECO_0000203 NP1077146.RAiNQbWxO8GelGfe6qVtYQy-1fi556a3rUp1ziZypEEVg130_provenance.