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- source_evidence_literature type ECO_0000212 NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_assertion description "[Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_assertion evidence source_evidence_literature NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_assertion SIO_000772 11220749 NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_assertion wasDerivedFrom befree-2016 NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_assertion wasGeneratedBy ECO_0000203 NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.
- befree-2016 importedOn "2016-02-19" NP309176.RAnp14-3wKe90PpzDIbVNFq7cSBMYd8i5OTBs7FIjnVSo130_provenance.