NP532428.RANITm-z1Hlxlsk-GHJjnbykjN-gHf5T09jRJ kk6bjUY
has assertion: NP532428.RANITm-z1Hlxlsk-GHJjnbykjN-gHf5T09jRJ kk6bjUY130 assertion
has provenance: NP532428.RANITm-z1Hlxlsk-GHJjnbykjN-gHf5T09jRJ kk6bjUY130 provenance
has publication info: NP532428.RANITm-z1Hlxlsk-GHJjnbykjN-gHf5T09jRJ kk6bjUY130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:45:46+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

NP532428.RANITm-z1Hlxlsk-GHJjnbykjN-gHf5T09jRJ kk6bjUY130 assertion
type: Assertion
description: [While there is no evidence for a significant association of several common lipoprotein-related genetic variants with carotid IMT, our results are consistent with the previously reported role of CETP and LPL genetic variants in cardiovascular risk and the possible modulation of the association between hypertension and carotid IMT by APOCIII Sst-1 variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16430904
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