Public Schema V2 · Skeletal Muscle Census V1
KM594
DISEASE_ASSOCIATED_REFERENCE · stable entity ID: SM-ENT-021
Provenance and Evidence
- Species
- Homo sapiens
- Tissue origin
- Human skeletal muscle, limb-girdle muscular dystrophy context
- Provenance summary
- Cells-Myoline disease myoblast panel; SM-SRC-005
- Evidence summary
- Cells-Myoline disease myoblast panel; SM-SRC-005
- Identity caveat
- IDENTITY_PROVISIONAL
- Public omics readiness
- NOT ASSESSED
Relationships
No parent relationship recorded.
Disease Applications
No curated disease-application evidence is recorded for KM594.
Disease application evidence describes documented experimental use. It does not change model identity, database role, physiological relevance, Disease Fidelity, or overall model ranking.
Physiological Relevance
No formal PR assessment available in PUBLIC_RC1. This does not imply low relevance, failure, or a recommendation against the model.
Uncertainty and Limitations
- SM HOLD PROVENANCE OR BOUNDARY — HOLD remains explicit and is not EXCLUDE.
Key limitations
- Provenance is incomplete or provisional in the frozen state.
- Structured uncertainty is retained from the frozen adjudication.
Analysis layers
Physiological Relevance and Disease Fidelity are separate analysis layers. No overall score or ranking is generated by this page.
- Physiological Relevance
- NOT_ASSESSED
- Disease Fidelity
- NOT_ASSESSED
- Availability
- NOT AVAILABLE
Skeletal Muscle V1 scientific context
- Coverage
- 0 adequate · 4 partial · 1 under-covered
- Saturation
- SATURATION LIMITED BY MODEL ECOSYSTEM
- Module state
- FROZEN
These module-level statements preserve the frozen scientific limitation context; they do not rank or reclassify this entity.