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{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/25157627","sourcedb":"@dpavot","sourceid":"25157627","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/25157627","text":"Though KRT5 has been identified to be the causal gene of DDD, the heterogeneity of this disease was displayed: for example, POFUT1 and POGLUT1 were recently identified and confirmed to be additional pathogenic genes of DDD.","tracks":[{"project":"PGR-UNK","denotations":[{"id":"T1","span":{"begin":7,"end":11},"obj":"3852"},{"id":"T2","span":{"begin":66,"end":79},"obj":"HP:0001425"}],"relations":[{"id":"R1","pred":"unknown","subj":"T1","obj":"T2"}],"attributes":[{"subj":"T1","pred":"source","obj":"PGR-UNK"},{"subj":"T2","pred":"source","obj":"PGR-UNK"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PGR-UNK","color":"#93ebec","default":true}]}]}}