Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_assertion description "[Mutations in NKX2.1, NKX2.5, FOXE1 and PAX8 genes, encoding for transcription factors involved in the development of the thyroid gland, have been identified in a minority of patients with syndromic and non-syndromic congenital hypothyroidism (CH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_assertion evidence source_evidence_literature NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_assertion SIO_000772 17468187 NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_assertion wasDerivedFrom befree-2016 NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_assertion wasGeneratedBy ECO_0000203 NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP607272.RAUzqjrwh4XKDEUFl79SkO4b5ya3eP_ESv_Mar4UCZQ8Y130_provenance.