Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_assertion description "[A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_assertion evidence source_evidence_literature NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_assertion SIO_000772 14684684 NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_assertion wasDerivedFrom befree-2016 NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_assertion wasGeneratedBy ECO_0000203 NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.
- befree-2016 importedOn "2016-02-19" NP425264.RAWVCQ4yhN22hxSR002yGykJ6PC1plKtmCP5976L1W4nE130_provenance.