Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion type Assertion NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_head.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion description "[The FOXE1 gene was screened for mutations in a cohort of 34 unrelated patients with congenital hypothyroidism, 14 of whom had thyroid dysgenesis and 18 were normal (the thyroid status for 2 patients was unknown).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_provenance.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion evidence source_evidence_literature NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_provenance.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion SIO_000772 20094846 NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_provenance.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion wasDerivedFrom befree-20150227 NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_provenance.
- NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_assertion wasGeneratedBy ECO_0000203 NP404842.RAYVcecLYW_Y2PEZk1pVxUzKd6nYGnLYC4Z3ZTYKZLGyk130_provenance.