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- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion type Assertion NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_head.
- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion wasGeneratedBy ECO_0000203 NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_provenance.
- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion wasDerivedFrom befree-20150227 NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_provenance.
- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion SIO_000772 9270600 NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_provenance.
- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion evidence source_evidence_literature NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_provenance.
- NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_assertion description "[Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355588.RAD-M8fteuXCGNb6vq6EIku6AJjzsCP_XUIGkgQUr-4mQ130_provenance.