Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_assertion description "[Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_assertion evidence source_evidence_curated NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_assertion SIO_000772 10594761 NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_assertion wasDerivedFrom uniprot-2016 NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_assertion wasGeneratedBy ECO_0000218 NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP532.RANSFQJP-h8Nt4yNpad9tQzN3adffSNFW68DOs2t_XQLs130_provenance.