Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion> ?p ?o ?g. }
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- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion type Assertion NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_head.
- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_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." NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_provenance.
- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion evidence source_evidence_literature NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_provenance.
- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion SIO_000772 17468187 NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_provenance.
- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion wasDerivedFrom befree-2016 NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_provenance.
- NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_assertion wasGeneratedBy ECO_0000203 NP607277.RAcfLwvjYGq7If_kcI7YJf52hNFIdpGAuNjDQOG2jMjuY130_provenance.