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- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion type Assertion NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_head.
- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion wasGeneratedBy ECO_0000203 NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_provenance.
- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion wasDerivedFrom befree-20150227 NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_provenance.
- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion SIO_000772 20660572 NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_provenance.
- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion evidence source_evidence_literature NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_provenance.
- NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_assertion description "[In the NET-Registry, 9/101 patients (8.9%) with ICTs had germline mutations, 8 in MEN1 and 1 in VHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376302.RALBTPz23rAZ-foHiFU7cSZLONGXGrjL-YL9V6ItXghXA130_provenance.