NP922644.RAtG-jDk4WEgY7Xus BTYgmQmogxXGt-ZSlpcKErPcVsg
has assertion: NP922644.RAtG-jDk4WEgY7Xus BTYgmQmogxXGt-ZSlpcKErPcVsg130 assertion
has provenance: NP922644.RAtG-jDk4WEgY7Xus BTYgmQmogxXGt-ZSlpcKErPcVsg130 provenance
has publication info: NP922644.RAtG-jDk4WEgY7Xus BTYgmQmogxXGt-ZSlpcKErPcVsg130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:48:42+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

NP922644.RAtG-jDk4WEgY7Xus BTYgmQmogxXGt-ZSlpcKErPcVsg130 assertion
type: Assertion
description: [Fourteen polymorphisms at or near 11 genes, including previously confirmed genes CFH, ARMS2/HTRA1, C2, C3, and CFI; recently reported AMD genes in the high-density lipoprotein cholesterol (HDL) pathway LIPC, ABCA1, CETP, and LPL; TIMP3/SYN3, a known ocular gene recently linked with AMD; and APOE, were assessed using logistic regression analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/21906714
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