RDF of MGI data pubmed

M K. Hajihosseini, et.al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98
http://rdf.ncbi.nlm.nih.gov/pubmed/11274405

M K. Hajihosseini, et.al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98(pubmed)

URI表示モード

M K. Hajihosseini, et.al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98

pubmed

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