Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion description "[Spectrum of mutations and sequence variants in the FALDH gene in patients with SjAPgren-Larsson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion evidence source_evidence_curated NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion SIO_000772 9829906 NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion wasDerivedFrom uniprot-20150221 NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion wasGeneratedBy ECO_0000218 NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_provenance.