Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion> ?p ?o ?g. }
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- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion type Assertion NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_head.
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- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion wasDerivedFrom uniprot-2016 NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion SIO_000772 8757036 NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion evidence source_evidence_curated NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion description "[Late-onset GM2 gangliosidosis is a variant form of Tay-Sachs disease characterized by onset of symptoms and signs in adolescence or in early adult life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.