Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_assertion wasGeneratedBy ECO_0000203 NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_assertion wasDerivedFrom befree-20140225 NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_assertion SIO_000772 18405873 NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_assertion evidence source_evidence_literature NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_assertion description "[In the present study, we show that truncating mutations of DYRK1A result in a clinical phenotype including microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP624231.RArkpsC_V9pxVjjW25mhV7tvsx-wYiMZhW59aoUvNoznM130_provenance.