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- source_evidence_literature type ECO_0000212 NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_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." NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_assertion evidence source_evidence_literature NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_assertion SIO_000772 11854319 NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_assertion wasDerivedFrom befree-20150227 NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_assertion wasGeneratedBy ECO_0000203 NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP739230.RAn_ZLJje4TTOmktsTCN5rFx48WFL3TdIwGXnbEuft8xQ130_provenance.