Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_assertion description "[The clinical and socio-demographic characteristics were not significantly different between the two groups; the genetic analysis revealed a significant correlation between the C/C genotype of 5-HT2A and TD (p=0.017).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_assertion evidence source_evidence_literature NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_assertion SIO_000772 15383158 NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_assertion wasDerivedFrom befree-2016 NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_assertion wasGeneratedBy ECO_0000203 NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.
- befree-2016 importedOn "2016-02-19" NP461074.RAOT3lUL0ILcXyqLscdWbY7JNPYL5lytvrNdgYU98D1uM130_provenance.