Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_assertion description "[Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_assertion evidence source_evidence_literature NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_assertion SIO_000772 7920658 NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_assertion wasDerivedFrom befree-2016 NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_assertion wasGeneratedBy ECO_0000203 NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1326998.RAmv15MMW4_lmh-EsM_DMxwB4FlIuClECM7YN0MbPhkyQ130_provenance.