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- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion type Assertion NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_head.
- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion description "[A novel mutation in the myotilin 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." NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_provenance.
- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion evidence source_evidence_literature NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_provenance.
- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion SIO_000772 16380616 NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_provenance.
- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion wasDerivedFrom lhgdn-20090331 NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_provenance.
- NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_assertion wasGeneratedBy ECO_0000203 NP198116.RAVc-IxmgB7M6aqFRX5ygqJAxCm7inrfyPRc1TROBf0DQ130_provenance.