Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP791783.RAD3pszTkqOiM-f7ixL5IYCWLO0_kmSdePRcTMY_u0RMc130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791783.RAD3pszTkqOiM-f7ixL5IYCWLO0_kmSdePRcTMY_u0RMc130_provenance.
• NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
• NP469533.RAt6q3eAKIvfXLvA4NVCIABLUlIVqwgtatJCZSSnM2AcM130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469533.RAt6q3eAKIvfXLvA4NVCIABLUlIVqwgtatJCZSSnM2AcM130_provenance.
• NP990124.RAXe6HFEFZZIGhxAQTVNVBHUDYn54T_PvlHCZeRXlshT4130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990124.RAXe6HFEFZZIGhxAQTVNVBHUDYn54T_PvlHCZeRXlshT4130_provenance.
• assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_provenance.
• NP1084877.RAOQXoxD39mMC-O6V9u5vKN_qW8MeA2BQjkYmFckNK-hM130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084877.RAOQXoxD39mMC-O6V9u5vKN_qW8MeA2BQjkYmFckNK-hM130_provenance.
• NP978343.RAPpPM5xSlXJ09a96jCmcTG6uP8NAbsaHDowOy64gn74Y130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978343.RAPpPM5xSlXJ09a96jCmcTG6uP8NAbsaHDowOy64gn74Y130_provenance.
• NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_provenance.
• NP1084876.RA1WRHJdyL6Olf7pFL1yt7yHwIRnjGFLd9urGZje0Scn0130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1084876.RA1WRHJdyL6Olf7pFL1yt7yHwIRnjGFLd9urGZje0Scn0130_provenance.