Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_assertion description "[These findings confirm that genetic variability in HTR(2A) contributes a small but significant degree of risk for the expression of TD, particularly in older patients and specifically for the non-orofacial (limb-truncal) type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_assertion evidence source_evidence_literature NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_assertion SIO_000772 15857569 NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_assertion wasDerivedFrom befree-2016 NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_assertion wasGeneratedBy ECO_0000203 NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.
- befree-2016 importedOn "2016-02-19" NP491862.RAPwBGQ4X_NVlV8WnUEEQL1odqNR-E2dipnEaA6AEPpok130_provenance.