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- source_evidence_literature type ECO_0000212 NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_assertion description "[Mutations in human GLIS3 have been implicated in a syndrome characterized by neonatal diabetes and congenital hypothyroidism (NDH) and in some patients accompanied by polycystic kidney disease, glaucoma, and liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_assertion evidence source_evidence_literature NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_assertion SIO_000772 20865670 NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_assertion wasDerivedFrom befree-2016 NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_assertion wasGeneratedBy ECO_0000203 NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.
- befree-2016 importedOn "2016-02-19" NP841624.RAi2jhT1N4b-8lvhAzh9mig4podhkxnSHCkhDzExa9-48130_provenance.