$('#metabolite-pathway-links'). html('
Name<\/th>SMPDB/PathBank<\/th>KEGG<\/th>
Hyperornithinemia-hyperammonemia-homocitrullinuria [HHH-syndrome]<\/td>\"Thumb\"<\/a>\"Thumb?image<\/a>\"Thumb?image<\/a><\/td>Not Available<\/span><\/td><\/tr>
Hyperprolinemia Type I<\/td>\"Thumb\"<\/a>\"Thumb?image<\/a>\"Thumb?image<\/a><\/td>Not Available<\/span><\/td><\/tr>
Hyperprolinemia Type II<\/td>\"Thumb\"<\/a>\"Thumb?image<\/a>\"Thumb?image<\/a><\/td>Not Available<\/span><\/td><\/tr>
L-arginine:glycine amidinotransferase deficiency<\/td>\"Thumb\"<\/a>\"Thumb?image<\/a>\"Thumb?image<\/a><\/td>Not Available<\/span><\/td><\/tr>
Ornithine Aminotransferase Deficiency (OAT Deficiency)<\/td>\"Thumb\"<\/a>\"Thumb?image<\/a>\"Thumb?image<\/a><\/td>Not Available<\/span><\/td><\/tr><\/tbody><\/table>