Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion> ?p ?o ?g. }
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- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion type Assertion NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_head.
- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion wasGeneratedBy ECO_0000203 NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_provenance.
- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion wasDerivedFrom befree-20150227 NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_provenance.
- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion SIO_000772 17199441 NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_provenance.
- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion evidence source_evidence_literature NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_provenance.
- NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_assertion description "[A novel mutation in the thyrotropin (thyroid-stimulating hormone) receptor gene in a case of congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760494.RARO__VXQa4ObbSjBSCvkvLR7KPwoviQQcNrLfD7x60dA130_provenance.