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- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion type Assertion NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_head.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion wasGeneratedBy ECO_0000203 NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion wasDerivedFrom gad-20150221 NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion SIO_000772 8755644 NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion evidence source_evidence_literature NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.
- NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_assertion description "[Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191396.RATPl_dfQKbpHZu1WH4euUtJvjd60uO8Dv3xI_BI9DI6s130_provenance.