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http://purl.uniprot.org/citations/7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7749225http://www.w3.org/2000/01/rdf-schema#comment"Neuromuscular degeneration, nmd, is a spontaneous autosomal recessive mutation in the mouse producing progressive hindlimb impairment caused by spinal muscular atrophy. We used an intersubspecific intercross between B6.BKs-nmd2J/+ and Mus musculus castaneus (CAST/Ei) to map the nmd mutation to mouse Chromosome (Chr) 19 with the most likely gene order: nmd-(D19Sel2, Pygm)-Cntf-Pomc2-D19Mit16-Cyp2c-Got1. nmd maps near muscle deficient, mdf, and has a very similar clinical phenotype, but allele tests and histological differences suggest that nmd is a distinct mutation at a different locus. Although closely linked, nmd recombined with the candidate genes muscle glycogen phosphorylase, Pygm, and ciliary neurotrophic factor, Cntf."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.org/dc/terms/identifier"doi:10.1007/bf00293010"xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/author"Bronson R.T."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/author"Johnson K.R."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/author"Davisson M.T."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/author"Cook S.A."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/date"1995"xsd:gYear
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/name"Mamm Genome"xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/pages"187-191"xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/title"Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration."xsd:string
http://purl.uniprot.org/citations/7749225http://purl.uniprot.org/core/volume"6"xsd:string
http://purl.uniprot.org/citations/7749225http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7749225
http://purl.uniprot.org/citations/7749225http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7749225
http://purl.uniprot.org/uniprot/#_A0A0B4J1E3-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_D3Z5P5-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_D6RFT3-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_F7ALS6-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_E9PUM3-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_H3BLM0-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_Q64458-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_P51642-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_Q3UT49-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_P05201-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225
http://purl.uniprot.org/uniprot/#_Q3UEF2-mappedCitation-7749225http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7749225