Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion> ?p ?o ?g. }
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- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion type Assertion NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_head.
- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_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." NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_provenance.
- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion evidence source_evidence_literature NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_provenance.
- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion SIO_000772 19429092 NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_provenance.
- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion wasDerivedFrom befree-20150227 NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_provenance.
- NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_assertion wasGeneratedBy ECO_0000203 NP792166.RAl8hl2D5B-Y76pV4-jm6OOmiR-4U3BqnddS8A-vLasm8130_provenance.