Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_assertion wasGeneratedBy ECO_0000218 NP9102.RASu3w3_MoCe3ZkSAsAjUdnNilFpyYugc-jBOA7kNlE38130_provenance.
- 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.