NP71379.RA6vjDhB wTjWfCZiTc-0kHVCwtj-hyqI4qcJRVV cQQ0
type: Nanopublication
has assertion: NP71379.RA6vjDhB wTjWfCZiTc-0kHVCwtj-hyqI4qcJRVV cQQ0130 assertion
has provenance: NP71379.RA6vjDhB wTjWfCZiTc-0kHVCwtj-hyqI4qcJRVV cQQ0130 provenance
has publication info: NP71379.RA6vjDhB wTjWfCZiTc-0kHVCwtj-hyqI4qcJRVV cQQ0130 publicationInfo
created: 2016-05-13T12:42:20+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

NP71379.RA6vjDhB wTjWfCZiTc-0kHVCwtj-hyqI4qcJRVV cQQ0130 assertion
type: Assertion
description: [We conclude that women homozygous for the Sp1 polymorphism are at significantly increased risk of excess rates of bone loss at the spine, but this effect may be nullified by the use of HRT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11547832
was generated by: ECO_0000203

gad-20150221
imported on: 2015-02-21

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

disgenetv3.0rdf
version: v4.0.0