NP1129423.RAipMkEGsRS IIcBJLrP7-EukFGGdhPdJMvYVtdWttgEU
has assertion: NP1129423.RAipMkEGsRS IIcBJLrP7-EukFGGdhPdJMvYVtdWttgEU130 assertion
has provenance: NP1129423.RAipMkEGsRS IIcBJLrP7-EukFGGdhPdJMvYVtdWttgEU130 provenance
has publication info: NP1129423.RAipMkEGsRS IIcBJLrP7-EukFGGdhPdJMvYVtdWttgEU130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:50:18+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

NP1129423.RAipMkEGsRS IIcBJLrP7-EukFGGdhPdJMvYVtdWttgEU130 assertion
type: Assertion
description: [We have reported previously that cranial neural-crest-specific inactivation of the homeobox gene Shox2, which is expressed in the mesenchymal cells of the maxilla-mandibular junction and later in the progenitor cells and perichondrium of the developing chondyle, leads to dysplasia and ankylosis of the TMJ and that replacement of the mouse Shox2 with the human SHOX gene rescues the dysplastic and ankylosis phenotypes but results in a prematurely worn out articular disc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/24248941
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