Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion> ?p ?o ?g. }
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- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion type Assertion NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_head.
- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_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." NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_provenance.
- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion evidence source_evidence_literature NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_provenance.
- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion SIO_000772 14510914 NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_provenance.
- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion wasDerivedFrom befree-2016 NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_provenance.
- NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_assertion wasGeneratedBy ECO_0000203 NP414646.RA09XQz1xdgu3Q3tZM5nmhLxELRxPxK-rAEr4uGYeXneU130_provenance.