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- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion type Assertion NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_head.
- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion description "[A novel mutation in the TTID gene results in the clinical and pathologic phenotype termed spheroid body myopathy. Mutations in this gene also cause limb-girdle muscular dystrophy 1A and are associated with myofibrillar myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_provenance.
- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion evidence source_evidence_literature NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_provenance.
- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion SIO_000772 16380616 NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_provenance.
- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion wasDerivedFrom befree-2016 NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_provenance.
- NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_assertion wasGeneratedBy ECO_0000203 NP528620.RA_dt2fLaR7eCPAwQBNmGZH8WLgZ88yIYeKi2EA4j2HX4130_provenance.