Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion> ?p ?o ?g. }
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- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion type Assertion NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_head.
- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion wasGeneratedBy ECO_0000203 NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_provenance.
- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion wasDerivedFrom befree-20140225 NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_provenance.
- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion SIO_000772 9590296 NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_provenance.
- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion evidence source_evidence_literature NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_provenance.
- NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_assertion description "[PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561301.RAPWrQ0rX_0sGo4qGrcaSJvfRhSB_e1tiPaYO5C4BmCTI130_provenance.