NP678018.RAbyL1VTJoa -gMg gWDsuFMYlbLl3-9Foht66-YJwKro
has assertion: NP678018.RAbyL1VTJoa -gMg gWDsuFMYlbLl3-9Foht66-YJwKro130 assertion
has provenance: NP678018.RAbyL1VTJoa -gMg gWDsuFMYlbLl3-9Foht66-YJwKro130 provenance
has publication info: NP678018.RAbyL1VTJoa -gMg gWDsuFMYlbLl3-9Foht66-YJwKro130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:38:49+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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: v2.1.0.0

NP678018.RAbyL1VTJoa -gMg gWDsuFMYlbLl3-9Foht66-YJwKro130 assertion
type: Assertion
description: [The enamelin gene (ENAM ), has been mapped to chromosome 4q21, to the same region as AIH2, and was recently shown to be mutated in patients with smooth and thin hypoplastic autosomal dominant AI (ADAI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/11978766
was generated by: ECO_0000203

befree-20140225
imported on: 2014-02-25

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

disgenetrdf
version: v2.1.0