Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion> ?p ?o ?g. }
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- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion type Assertion NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_head.
- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion wasGeneratedBy ECO_0000203 NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion wasDerivedFrom befree-20140225 NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion SIO_000772 14729820 NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion evidence source_evidence_literature NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_assertion description "[While mutations in the NDUFS3 gene thus result in Leigh syndrome, a dissimilar clinical phenotype is observed in mutations in the NDUFV2 and NDUFS2 genes, resulting in encephalomyopathy and cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.