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- source_evidence_literature type ECO_0000212 NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_assertion description "[Mutations in the peripherin/retinal degeneration slow (RDS) gene have been identified in patients with retinitis pigmentosa and pattern macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_assertion evidence source_evidence_literature NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_assertion SIO_000772 7862413 NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_assertion wasDerivedFrom befree-20150227 NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_assertion wasGeneratedBy ECO_0000203 NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761014.RAtTOQY2w1-4eKR7JwmTySeRJOZXxAsnXLHIJn7xnQWis130_provenance.