Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion type Assertion NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_head.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion description "[Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_provenance.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion evidence source_evidence_literature NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_provenance.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion SIO_000772 14510914 NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_provenance.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion wasDerivedFrom befree-20150227 NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_provenance.
- NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_assertion wasGeneratedBy ECO_0000203 NP697733.RAYSInwf6e4eV5ldvBkwtTdlW4512_NkID54bqn8A50eU130_provenance.