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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 COL1A1 fibrillar procollagens [extracellular region]

Class:IdDefinedSet:9015566
_displayNameDefective COL1A1 fibrillar procollagens [extracellular region]
_timestamp2017-08-10 14:12:16
compartment[Compartment:984] extracellular region
created[InstanceEdit:9015580] Varusai, Thawfeek, 2017-08-10
disease[Disease:9015256] osteogenesis imperfecta
hasMember
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 COL1A1 fibrillar procollagens
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9015614] R-HSA-9015566.1
(output)[BlackBoxEvent:9015574] Secretion of abnormal COL1A1 collagens [Homo sapiens]
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No pathways have been reviewed or authored by Defective COL1A1 fibrillar procollagens [extracellular region] (9015566)
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