Brain Transcriptome Database (BrainTx)http://rdf.ncbi.nlm.nih.gov/pubmed/

Melanie. Schütz, et.al., The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome., Human molecular genetics, 2011, 20
http://rdf.ncbi.nlm.nih.gov/pubmed/20926451

Melanie. Schütz, et.al., The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome., Human molecular genetics, 2011, 20

http://rdf.ncbi.nlm.nih.gov/pubmed/

トランスクリプトームデータ
http://rdf.ncbi.nlm.nih.gov/pubmed/
allele
http://purl.org/net/cito/citesAsAuthority
表現型アノテーション
http://purl.org/net/cito/citesAsAuthority