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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Defective C-linked procollagen type I trimer [endoplasmic reticulum lumen]

Class:IdComplex:9015571
_displayNameDefective C-linked procollagen type I trimer [endoplasmic reticulum lumen]
_timestamp2017-08-10 14:11:48
compartment[Compartment:17957] endoplasmic reticulum lumen
created[InstanceEdit:9015580] Varusai, Thawfeek, 2017-08-10
disease[Disease:9015256] osteogenesis imperfecta
hasComponent
isChimericFALSE
literatureReference[LiteratureReference:9015250] The human type I collagen mutation database
[LiteratureReference:9015589] Mutations in type I collagen genes resulting in osteogenesis imperfecta in humans
modified[InstanceEdit:9015624] Varusai, Thawfeek, 2017-08-10
nameDefective C-linked procollagen type I trimer
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9015604] R-HSA-9015571.1
(hasMember)[DefinedSet:9015586] Defective procollagen type I bind to form abnormal fibrillar collagens [endoplasmic reticulum lumen] [Homo sapiens]
[DefinedSet:9015591] Defective COL1A1 procollagen C-linked trimers [endoplasmic reticulum lumen] [Homo sapiens]
(output)[Reaction:9015565] Defective procollagen type I [Homo sapiens]
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