Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_assertion wasGeneratedBy ECO_0000203 NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_assertion wasDerivedFrom befree-2016 NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_assertion SIO_000772 8757036 NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_assertion evidence source_evidence_literature NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.
- NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_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." NP1355522.RAV03Qth3jC5secJP0NUL3M8QGqCMbWqTlCmTwT6xB68Y130_provenance.