Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion> ?p ?o ?g. }
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- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion type Assertion NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_head.
- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion description "[Multiple endocrine neoplasia 2a (MEN2a) syndrome is one of the rare genetic disorder where prophylactic thyroidectomy is recommended for RET mutation carriers due to increased risk for developing MTC during lifetime.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_provenance.
- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion evidence source_evidence_literature NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_provenance.
- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion SIO_000772 22715565 NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_provenance.
- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion wasDerivedFrom befree-20150227 NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_provenance.
- NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_assertion wasGeneratedBy ECO_0000203 NP599822.RA7z4u4d41JXRizj4NNJgO0hjtwygUXJiBgcC0NwDo5QY130_provenance.