NP253179.RATvU8J AIIHfpUFGcKELxlQR8-BXKPJ26Z THJDI29DA
type: Nanopublication
has assertion: NP253179.RATvU8J AIIHfpUFGcKELxlQR8-BXKPJ26Z THJDI29DA130 assertion
has provenance: NP253179.RATvU8J AIIHfpUFGcKELxlQR8-BXKPJ26Z THJDI29DA130 provenance
has publication info: NP253179.RATvU8J AIIHfpUFGcKELxlQR8-BXKPJ26Z THJDI29DA130 publicationInfo
created: 2016-05-13T12:43:41+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

NP253179.RATvU8J AIIHfpUFGcKELxlQR8-BXKPJ26Z THJDI29DA130 assertion
type: Assertion
description: [Surprisingly, immunohistochemical experiments using a polyclonal antiexcitatory amino acid transporter 2 antibody, showed a different localization of this protein in epilepsy derived tissue as compared to post mortem controls although glial markers such as glial fibrillary acidic protein and glutamine synthase showed similar patterns of staining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/10336123
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