Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_assertion description "[Urinary and plasma amines and amine metabolites were quantified in two individuals with Norrie disease resulting from a deletion in chromosomal region Xp11.3, recently reported to be associated with absence of the gene encoding monoamine oxidase (MAO)-A and nondetectable MAO-A activity in fibroblasts and MAO-B activity in platelets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_assertion evidence source_evidence_literature NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_assertion SIO_000772 2293615 NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_assertion wasDerivedFrom befree-20140225 NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_assertion wasGeneratedBy ECO_0000203 NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP380961.RA3W-36hd44F7dl7y25pdK4CiSgfch_1Mv7A9zI11MS8A130_provenance.