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- source_evidence_literature type ECO_0000212 NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_assertion description "[Clinical, functional and genetic analysis of twenty-four patients with chronic granulomatous disease - identification of eight novel mutations in CYBB and NCF2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_assertion evidence source_evidence_literature NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_assertion SIO_000772 22562447 NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_assertion wasDerivedFrom befree-2016 NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_assertion wasGeneratedBy ECO_0000203 NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP979995.RAUglTMkOyKVuL1nPCbef_37Xux2naLHd73l2TSbscXIM130_provenance.