NP1301671.RAgj8 yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM
has assertion: NP1301671.RAgj8 yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130 assertion
has provenance: NP1301671.RAgj8 yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130 provenance
has publication info: NP1301671.RAgj8 yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:51:36+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

NP1301671.RAgj8 yg62gPT-uGCMypYUPlQOQKYPoA-mMwWjLbKFfEM130 assertion
type: Assertion
description: [Unlike type I procollagen molecules synthesized by cells from most other infants with osteogenesis imperfecta type II which contain increased lysyl hydroxylation and hydroxylysyl glycosylation along the triple helical domain, the abnormal molecules synthesized by these cells are not overmodified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/3372508
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