Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_assertion wasGeneratedBy ECO_0000218 NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_assertion wasDerivedFrom uniprot-20150221 NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_assertion SIO_000772 8757036 NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_assertion evidence source_evidence_curated NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.
- NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_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." NP1186.RAscbCfEy9JL1JCs7fkjEPeBD-lRjgo0nZOHkyjWdImyk130_provenance.