http://rdf.disgenet.org/resource/nanopub/NP124263.RAW4omykOUVcsL_OIxprGnEqtMYvIK4jusoj-Th7mgl50
type: Nanopublication
created: 2016-05-13T12:42:44+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

http://rdf.disgenet.org/resource/nanopub/NP124263.RAW4omykOUVcsL_OIxprGnEqtMYvIK4jusoj-Th7mgl50130_assertion
type: Assertion
description: [To investigate the possible association of variations of the H2AX gene with spermatogenic impairment in humans, mutation screening of the entire coding region of this gene was carried out in 302 patients with azoospermia or severe oligospermia along with 198 normospermic controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18536151
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