Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_assertion description "[The G482T and G689T polymorphisms in the 3'-UTR of serotonin transporter (SLC6A4) are implicated in translational regulation and allelic variants may mediate susceptibility to attention-deficit-hyperactivity disorder (ADHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_assertion evidence source_evidence_literature NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_assertion SIO_000772 19429092 NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_assertion wasDerivedFrom befree-20150227 NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_assertion wasGeneratedBy ECO_0000203 NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP432541.RAuyYVEFrwQOPBM_hZ10IRy-xWWMi_TwrjA-TSpIRhnkY130_provenance.