Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion> ?p ?o ?g. }
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- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion type Assertion NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_head.
- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion description "[Familial cases of congenital hypothyroidism from thyroid dysgenesis (TD) (OMIM 218700) occur with a frequency 15-fold higher than by chance, FOXE1 is one of the candidate genes for this genetic predisposition and contains an alanine tract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_provenance.
- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion evidence source_evidence_literature NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_provenance.
- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion SIO_000772 17717707 NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_provenance.
- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion wasDerivedFrom befree-2016 NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_provenance.
- NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_assertion wasGeneratedBy ECO_0000203 NP626526.RAXwK5gAlom_mq7P1yxaFvOoSrtS6C9td72gk7oaPkBlw130_provenance.