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Explore connected evidence

Graph Explorer

Follow genes through disease annotations and ortholog candidates. Select a connection to inspect the source record.

Evidence format & Python client ↗

Loading species and snapshot information…

Evidence network

Start with a gene list to build your graph.

Begin with a gene list, or open a graph saved by BioWeaver or the Python client.

● Loaded gene○ Donor context◆ Annotation record▰ Disease▱ Reference― Curated┄ Inferred·· Negative

Connections describe source records, not causal pathways or a gene ranking.

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Inspect evidence

Select a node or connection

Every annotation keeps its original relation, references and donor records.

Original source record 
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Annotation records in this view

Select a record to find it in the network. The download includes every matching record, across all pages.

Input decisions & source snapshots 
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An empty source result means no matched record in this snapshot. It does not establish that nobody has studied the gene. Ortholog candidates come from the exported stringent subset.