Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_assertion description "[This study identified chaperone-responsive mutants that represent 56 of 713 known patient-derived CBS alleles and may serve as a basis for exploring pharmacological approaches aimed at correcting misfolding in homocystinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_assertion evidence source_evidence_literature NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_assertion SIO_000772 20490928 NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_assertion wasDerivedFrom befree-20150227 NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_assertion wasGeneratedBy ECO_0000203 NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP286716.RAvKMh86V6phIEqWt6PyiDILX0vFtiNKVdIRniSd3-MjA130_provenance.