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- source_evidence_literature type ECO_0000212 NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_assertion description "[Based on a nested-PCR approach and direct sequencing, a disease causing mutation at the SCA31 locus could be excluded for the German SCA4 kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_assertion evidence source_evidence_literature NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_assertion SIO_000772 21267591 NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_assertion wasDerivedFrom befree-2016 NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_assertion wasGeneratedBy ECO_0000203 NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.
- befree-2016 importedOn "2016-02-19" NP867790.RANp0X0-LkuHpyN0LjdF5RrHZWUIIUNFIHC3soE-h9_0g130_provenance.