Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_assertion description "[Further oxidation of this substrate by the fatty alcohol:nicotinamide-adenine dinucleotide oxidoreductase (FAO) enzyme complex, in which one component, ALDH3A2, is known to be mutated in Sj�gren-Larsson syndrome (characterized by ichthyosis and spastic paraplegia), would lead to 20-carboxy-(R)-trioxilin A3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_assertion evidence source_evidence_literature NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_assertion SIO_000772 16436457 NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_assertion wasDerivedFrom befree-2016 NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_assertion wasGeneratedBy ECO_0000203 NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.
- befree-2016 importedOn "2016-02-19" NP532883.RAKPpQmf_r_jRwMyUODVf_QEeD1tq6Jy8Hnz5zzzSaU8s130_provenance.