Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_assertion wasGeneratedBy ECO_0000218 NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_assertion wasDerivedFrom uniprot-20130724 NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_assertion SIO_000772 8757036 NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_assertion evidence source_evidence_curated NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_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." NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2989.RAdT_OP8WXnSlXf0vZ1MXqyTdFbC6ewSgim1LsB3iQzhg130_provenance.