PubMed:2120217 JSONTXT 29 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
2120217-0#19#29#gene7299 19-29 gene7299 denotes tyrosinase
2120217-0#39#62#diseaseC0078918 39-62 diseaseC0078918 denotes oculocutaneous albinism
2120217-0#94#104#gene7299 94-104 gene7299 denotes tyrosinase
2120217-1#0#10#gene7299 169-179 gene7299 denotes Tyrosinase
2120217-1#70#97#diseaseC0025521 239-266 diseaseC0025521 denotes inborn errors of metabolism
2120217-8#30#36#diseaseC0001916 1263-1269 diseaseC0001916 denotes albino
2120217-8#165#175#gene7299 1398-1408 gene7299 denotes tyrosinase
0#10#gene729970#97#diseaseC0025521 2120217-1#0#10#gene7299 2120217-1#70#97#diseaseC0025521 associated_with Tyrosinase,inborn errors of metabolism
165#175#gene729930#36#diseaseC0001916 2120217-8#165#175#gene7299 2120217-8#30#36#diseaseC0001916 associated_with tyrosinase,albino
19#29#gene729939#62#diseaseC0078918 2120217-0#19#29#gene7299 2120217-0#39#62#diseaseC0078918 associated_with tyrosinase,oculocutaneous albinism
94#104#gene729939#62#diseaseC0078918 2120217-0#94#104#gene7299 2120217-0#39#62#diseaseC0078918 associated_with tyrosinase,oculocutaneous albinism