Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_assertion description "[We did not find main effects of the COMT and SLC6A2 NET1 gene haplotypes on any ADHD symptom severity score.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_assertion evidence source_evidence_literature NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_assertion SIO_000772 17994190 NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_assertion wasDerivedFrom befree-20140225 NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_assertion wasGeneratedBy ECO_0000203 NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP871129.RAkz45uGhGCC-Er9ZF4VZrPEpIOnZS_v_RtoNhvwisEoM130_provenance.