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- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion type Assertion NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_head.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion description "[We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion evidence source_evidence_literature NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion SIO_000772 18765513 NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion wasDerivedFrom befree-20150227 NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.
- NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_assertion wasGeneratedBy ECO_0000203 NP897390.RAK92QJ8-6PeyZQLpRYUF89cUikudSPrlGnTZdhNJ8DIM130_provenance.