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- source_evidence_literature type ECO_0000212 NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_assertion wasGeneratedBy ECO_0000203 NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_assertion wasDerivedFrom lhgdn-20090331 NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_assertion SIO_000772 15786463 NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_assertion evidence source_evidence_literature NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.
- NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_assertion description "[TRIM32 mutation found in the sarcotubular myopathy patients is identical to the causative mutation for LGMD2H (D487N)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198141.RAvWrj8cLEwxQmJMjfEO_skD1mbzXJk_zCnK0j0mRyfCE130_provenance.