RDF of MGI datapubmed

Benjamin M. Kriederman, et.al., FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome., Human molecular genetics, 2003, 12
http://rdf.ncbi.nlm.nih.gov/pubmed/12719382

Benjamin M. Kriederman, et.al., FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome., Human molecular genetics, 2003, 12

pubmed

表現型アノテーション