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- source_evidence_literature type ECO_0000212 NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_assertion wasGeneratedBy ECO_0000203 NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_assertion wasDerivedFrom befree-20150227 NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_assertion SIO_000772 22015311 NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_assertion evidence source_evidence_literature NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.
- NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_assertion description "[Mutations in the optineurin gene (OPTN) have been reported in rare familial and sporadic amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837089.RAcjsWYlAT-kfl0JP1zlnDVvnpZzXk2_f0M6z8YuuJ5hY130_provenance.