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- source_evidence_literature type ECO_0000212 NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_assertion description "[To describe patients with cone dystrophy and supernormal rod electroretinogram (ERG) and search for mutations in the recently described KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_assertion evidence source_evidence_literature NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_assertion SIO_000772 18400204 NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_assertion wasDerivedFrom befree-20140225 NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_assertion wasGeneratedBy ECO_0000203 NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP710700.RAHlhEY1Ou-6pJ4VPWHGitfD0w8YcG_pynPi2aeD5CB3Q130_provenance.