NP515613.RAVhn-Lw wyQ10nlld gfvprMLyDdyGQkLhhahczwpCo
type: Nanopublication
has assertion: NP515613.RAVhn-Lw wyQ10nlld gfvprMLyDdyGQkLhhahczwpCo130 assertion
has provenance: NP515613.RAVhn-Lw wyQ10nlld gfvprMLyDdyGQkLhhahczwpCo130 provenance
has publication info: NP515613.RAVhn-Lw wyQ10nlld gfvprMLyDdyGQkLhhahczwpCo130 publicationInfo
created: 2016-05-13T12:45:38+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

NP515613.RAVhn-Lw wyQ10nlld gfvprMLyDdyGQkLhhahczwpCo130 assertion
type: Assertion
description: [The FMR1 gene should be analyzed in patients with tall stature and mental retardation, and in these patients the NSD1 gene can be considered whenever some features of Sotos syndrome do exist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16192740
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