Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion> ?p ?o ?g. }
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- NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_assertion type Assertion NP6329.RANyHLTexLovJNZ7ukF6pUuU-QOvgFi-MRdUERvjoCPkg130_head.
- 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.