Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP570242.RAn1M1HWBr7ZJRZS6MpWRXd2bOkmwd5LsSRUN_pSWt39Y130_provenance.