NP792134.RAQwXQR Xq9outNhiCey Q4 zZ9XRDdnJ8F8-SQw8pvrM
type: Nanopublication
has assertion: NP792134.RAQwXQR Xq9outNhiCey Q4 zZ9XRDdnJ8F8-SQw8pvrM130 assertion
has provenance: NP792134.RAQwXQR Xq9outNhiCey Q4 zZ9XRDdnJ8F8-SQw8pvrM130 provenance
has publication info: NP792134.RAQwXQR Xq9outNhiCey Q4 zZ9XRDdnJ8F8-SQw8pvrM130 publicationInfo
created: 2016-05-13T12:47:44+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

NP792134.RAQwXQR Xq9outNhiCey Q4 zZ9XRDdnJ8F8-SQw8pvrM130 assertion
type: Assertion
description: [The primary focus has been on SNPs in dopamine and serotonin receptor genes: persuasive meta-analytic evidence exists for an effect of the dopamine D2 and D3 receptor genes (DRD2 and DRD3) in risk for tardive dyskinesia (TD) and for an effect of variation at the 5-HT2C receptor gene (HTR2C) for liability to APD-induced weight gain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/20135898
was generated by: ECO_0000203

befree-2016
imported on: 2016-02-19

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0