Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion> ?p ?o ?g. }
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- NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_assertion type Assertion NP2837.RAj4h2eJVQhE22hz8pRPxp5sbSEzEYHYGbD-gkDtD6WNc130_head.
- 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.