Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_assertion description "[These results confirm that the hemizygous COMT Val(158)Met genotype impacts upon cognition in children with 22q11DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_assertion evidence source_evidence_literature NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_assertion SIO_000772 16542388 NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_assertion wasDerivedFrom befree-20140225 NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_assertion wasGeneratedBy ECO_0000203 NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP175823.RAyexfAqwH-_0QHcIF-3GolTNAPTjlVhiCwbLWEDgEeG4130_provenance.