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- source_evidence_literature type ECO_0000212 NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_assertion description "[After correcting for multiple testing, the association between DRD4.2 and BP dropped to insignificance; however, the evidence of an association between the DRD4.2 allele and UP (p < .001) and the combined group (p < .001) remained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_assertion evidence source_evidence_literature NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_assertion SIO_000772 15860340 NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_assertion wasDerivedFrom befree-2016 NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_assertion wasGeneratedBy ECO_0000203 NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP492019.RA27FH-BglTNcn6eZBR5StXp4ariE9fNBI7HWelQGnYIM130_provenance.