Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP715226.RA9rbXgYfyiLdz8l2OtqIRTHjFVqfjRR5xyJan2BH-tSI130_provenance.