http://rdf.disgenet.org/resource/nanopub/NP77507.RAuEP6LRmf47cdePHmdyLMW6ntnON-TI6XoDbFZuwSvBo
type: Nanopublication
created: 2016-05-13T12:42:23+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/NP77507.RAuEP6LRmf47cdePHmdyLMW6ntnON-TI6XoDbFZuwSvBo130_assertion
type: Assertion
description: [Although the number of patients evaluated was small and we cannot exclude the presence of mutation in other regions, for example, the promoter region of the AMH or AMHR2 genes are rare in Japanese women with idiopathic POF and PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12477536
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