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- source_evidence_literature type ECO_0000212 NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_assertion description "[We investigated two single-nucleotide polymorphisms (SNPs) in PDCD1 and five polymorphisms in CTLA4 in 102 patients with AAV and 188 healthy controls (HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_assertion evidence source_evidence_literature NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_assertion SIO_000772 18448390 NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_assertion wasDerivedFrom befree-20150227 NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_assertion wasGeneratedBy ECO_0000203 NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP612930.RAgSB6jUqFicKFjCOihmExB9-llOiOWt98M0LRBDk34v0130_provenance.