NP976696.RA5UY lti IsB3R 6ZkHbgC 2INUAUsu35 uabZdtrmJM
has assertion: NP976696.RA5UY lti IsB3R 6ZkHbgC 2INUAUsu35 uabZdtrmJM130 assertion
has provenance: NP976696.RA5UY lti IsB3R 6ZkHbgC 2INUAUsu35 uabZdtrmJM130 provenance
has publication info: NP976696.RA5UY lti IsB3R 6ZkHbgC 2INUAUsu35 uabZdtrmJM130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:49:07+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

NP976696.RA5UY lti IsB3R 6ZkHbgC 2INUAUsu35 uabZdtrmJM130 assertion
type: Assertion
description: [Although the majority of evidence supports associations between the SOD2 Ala16Val SNP and diseases such as breast, prostate and lung cancers, diabetes and cardiovascular disease, the presence of the SOD2 Ala16Val SNP confers only a small, clinically insignificant reduction (if any) in the risk of these diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/22525041
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