Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_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." NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_assertion evidence source_evidence_literature NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_assertion SIO_000772 16436457 NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_assertion wasDerivedFrom befree-20150227 NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_assertion wasGeneratedBy ECO_0000203 NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800000.RAgsNOjodjKhz_b6QDFyAgHbW8KJp5v9LYU-vnoP_1_sI130_provenance.