Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_assertion description "[To the best of our knowledge, this is the first report showing an association between functional polymorphisms in NR3C1 and ADHD, providing genetic evidence for involvement of the HPA axis in the disorder and treatment response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_assertion evidence source_evidence_literature NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_assertion SIO_000772 23055001 NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_assertion wasDerivedFrom befree-2016 NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_assertion wasGeneratedBy ECO_0000203 NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.
- befree-2016 importedOn "2016-02-19" NP1019905.RApNobpNLCdRiLlbeUxtdMxTGtxWkVF-9Hfft_654Awog130_provenance.