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- source_evidence_literature type ECO_0000212 NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_assertion description "[We suggest that specific point mutations in the CO1 and CO2 genes cause the CO defect in AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_assertion evidence source_evidence_literature NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_assertion SIO_000772 9114023 NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_assertion wasDerivedFrom befree-2016 NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_assertion wasGeneratedBy ECO_0000203 NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1371110.RAgDLrnN1mXEKMLrno9TZNbUtjkyK8cb-b16HfeXLwSBI130_provenance.