Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion> ?p ?o ?g. }
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- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion type Assertion NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_head.
- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion description "[No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with attention-deficit-hyperactivity disorder (ADHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_provenance.
- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion evidence source_evidence_literature NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_provenance.
- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion SIO_000772 19429092 NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_provenance.
- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion wasDerivedFrom befree-2016 NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_provenance.
- NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_assertion wasGeneratedBy ECO_0000203 NP737706.RACP0vbQE4vE-xAbh6oKrb7_62mIG-1KTp8Pnp1Cp2HDk130_provenance.