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- source_evidence_literature type ECO_0000212 NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_assertion description "[A mutation in the CYBB gene encoding gp91(phox) leads to X-linked recessive CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_assertion evidence source_evidence_literature NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_assertion SIO_000772 23910690 NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_assertion wasDerivedFrom befree-20150227 NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_assertion wasGeneratedBy ECO_0000203 NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP338882.RAb_-nodWKm7eP7XYFfXRHUfPan5rXJi0iHC-31LSY9bA130_provenance.