Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_assertion description "[Therefore, the unfavorable outcome in patients with CH, especially those with choreoathetosis and pulmonary symptoms, can be explained by mutations in the NKX2-1 gene rather than by hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_assertion evidence source_evidence_literature NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_assertion SIO_000772 11854319 NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_assertion wasDerivedFrom befree-2016 NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_assertion wasGeneratedBy ECO_0000203 NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.
- befree-2016 importedOn "2016-02-19" NP345720.RARxpcVCzEmxspg6oGwjDqUXmbBQaAjtn3Nyrrj_0s0uM130_provenance.