Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion> ?p ?o ?g. }
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- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion type Assertion NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_head.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion wasGeneratedBy ECO_0000203 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion wasDerivedFrom befree-20140225 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion SIO_000772 18528812 NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion evidence source_evidence_literature NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.
- NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_assertion description "[Constitutively activating thyrotropin receptor (TSHR) germline mutations have been identified as a molecular cause of congenital hyperthyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609469.RAzP2N5Bbi9Y-tTikmfsXalV8FnO5Qelwuix3uflxHErA130_provenance.