Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion description "[A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion evidence source_evidence_curated NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion SIO_000772 17646629 NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion wasDerivedFrom uniprot-20130724 NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion wasGeneratedBy ECO_0000218 NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_provenance.