Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion type Assertion NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_head.
- 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.
- NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion evidence source_evidence_literature NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_provenance.
- NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion SIO_000772 23754960 NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_provenance.
- NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion wasDerivedFrom befree-2016 NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_provenance.
- NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_assertion wasGeneratedBy ECO_0000203 NP1084874.RA_Jz9JILEtojjsUoYHbs1x5yh0N1QBaEHk_95w2bu8YE130_provenance.