Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion> ?p ?o ?g. }
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- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion type Assertion NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_head.
- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion description "[In patients with congenital hypothyroidism (CH), the autosomal recessive inheritance of mutations of thyroid peroxidase, thyroglobulin and the NIS and pendrin genes encoding for sodium iodide transporters has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_provenance.
- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion evidence source_evidence_literature NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_provenance.
- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion SIO_000772 10895037 NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_provenance.
- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion wasDerivedFrom befree-20150227 NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_provenance.
- NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_assertion wasGeneratedBy ECO_0000203 NP697732.RAYEVlQtX5T0o82CRIurH2cfdmw4W_B4HWL9dYRw0RxD8130_provenance.