RDF of MGI data pubmed

T F. Tsai, et.al., Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome., Human molecular genetics, 1999, 8
http://rdf.ncbi.nlm.nih.gov/pubmed/10400982

T F. Tsai, et.al., Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome., Human molecular genetics, 1999, 8(pubmed)

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T F. Tsai, et.al., Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome., Human molecular genetics, 1999, 8

pubmed

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