http://rdf.disgenet.org/resource/nanopub/NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k
type: Nanopublication
created: 2016-05-13T12:43:26+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/NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion
type: Assertion
description: [An analysis of frequency distribution of the Gln233Arg polymorphism in the leptin receptor gene in children with acute lymphoblastic or acute myeloblastic leukemia showed lack of differences between the patients and 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/17072067
was generated by: ECO_0000203

lhgdn-20090331
imported on: 2009-03-31

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

disgenetv3.0rdf
version: v4.0.0