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- source_evidence_literature type ECO_0000212 NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_assertion description "[Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_assertion evidence source_evidence_literature NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_assertion SIO_000772 20932283 NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_assertion wasDerivedFrom befree-20140225 NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_assertion wasGeneratedBy ECO_0000203 NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP586489.RA3PXBZkHOtBzTek7iK8uWES0lx0i5Eo10oS52BmZvgnc130_provenance.