Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- befree-2016 importedOn "2016-02-19" NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_assertion wasGeneratedBy ECO_0000203 NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_assertion wasDerivedFrom befree-2016 NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_assertion SIO_000772 15055360 NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_assertion evidence source_evidence_literature NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.
- NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_assertion description "[TPO abnormality is considered to be a major cause of congenital hypothyroidism (CH) with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437861.RAkR1sZgRpuAr7Uy7xRhhOXPPNDX33N0aC-2JJrcWSxQc130_provenance.