Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_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." NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_assertion evidence source_evidence_literature NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_assertion SIO_000772 16436457 NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_assertion wasDerivedFrom befree-20140225 NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_assertion wasGeneratedBy ECO_0000203 NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833025.RAgH_SRpwTW-q4CHqnliEl0BZQyV_cXzuNxbCJQyOOfeI130_provenance.