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- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion type Assertion NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_head.
- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion wasGeneratedBy ECO_0000203 NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_provenance.
- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion wasDerivedFrom befree-20150227 NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_provenance.
- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion SIO_000772 20234391 NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_provenance.
- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion evidence source_evidence_literature NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_provenance.
- NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_assertion description "[As these symptoms are a subset of those observed in disorders of dystroglycan glycosylation (muscle-eye-brain disease and Warker-Warburg syndrome), we assess the likely contribution to her phenotype of her heterogosity for a null mutation of DAG1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346802.RAXbmdaaukr9k38F-Maa9yQKWsIZIkEtDLJZyppxnmf14130_provenance.