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L-tryptophan correlated with condition Hereditary Autosomal Dominant Spastic Paraplegia (Knowledge Graph Assertion)

Target:

Hereditary Autosomal Dominant Spastic Paraplegia

Disease Or Phenotype (Entity type)

Source:

L-tryptophan

Metabolite (Entity type)

Relation:

correlated with condition

Knowledge Graph Relation (Entity type)

Dcc Asset:

MW.zip

Processed File (Entity type)

Dcc:

Metabolomics

DCC (Entity type)

Sab:MW

Results found

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Community

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@CFDE Workbench 2025

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

Consortium

Community

Resources

The CFDE Workbench is actively being developed and maintained by the CFDE Data Resource Center (DRC).The DRC is funded by OT2OD036435 from the Common Fund at the National Institutes of Health.

@CFDE Workbench 2025

This repository is under review for potential modification in compliance with Administration directives.