Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion> ?p ?o ?g. }
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- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion type Assertion NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_head.
- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion description "[Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_provenance.
- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion evidence source_evidence_literature NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_provenance.
- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion SIO_000772 20094846 NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_provenance.
- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion wasDerivedFrom gad-20150221 NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_provenance.
- NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_assertion wasGeneratedBy ECO_0000203 NP139767.RAQiM2eaO3Ku-2sMKtY6F-BQmkb9Ndf-lr8a3zEvjqChs130_provenance.