Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion> ?p ?o ?g. }
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- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion type Assertion NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_head.
- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion description "[The occurrence of thyroid carcinoma in patients with congenital hypothyroidism (CH) caused by dyshormonogenesis is very rare, and has only been reported in one patient harboring mutations in the thyroid peroxidase (TPO) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_provenance.
- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion evidence source_evidence_literature NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_provenance.
- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion SIO_000772 22435912 NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_provenance.
- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion wasDerivedFrom befree-2016 NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_provenance.
- NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_assertion wasGeneratedBy ECO_0000203 NP969382.RAhO0v63tEbZxsZPrNcZ7foZXw7wT9nc3TlnVU1A03pM0130_provenance.