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- source_evidence_literature type ECO_0000212 NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_assertion evidence source_evidence_literature NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_assertion SIO_000772 18445003 NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_assertion wasDerivedFrom befree-2016 NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_assertion wasGeneratedBy ECO_0000203 NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.
- befree-2016 importedOn "2016-02-19" NP668447.RAUr1bNrI4_01upAq5HJSNHVWRtT0n6TMqjA4ghvHtmKc130_provenance.