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- NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion type Assertion NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_head.
- 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.
- NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion evidence source_evidence_literature NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_provenance.
- NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion SIO_000772 23754960 NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_provenance.
- NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion wasDerivedFrom befree-20150227 NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_provenance.
- NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_assertion wasGeneratedBy ECO_0000203 NP980131.RAqNFemEOCPUpRqHqfw0VArudKLIJ2T_KDswIPw7pv20M130_provenance.