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- source_evidence_literature type ECO_0000212 NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_assertion description "[CTNNB1 mutation was only found in one OC case, whereas three of six (50%) ameloblastoma cases and two out of eight (25%) OC cases had APC mutations within the mutational cluster region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_assertion evidence source_evidence_literature NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_assertion SIO_000772 18486530 NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_assertion wasDerivedFrom befree-2016 NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_assertion wasGeneratedBy ECO_0000203 NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.
- befree-2016 importedOn "2016-02-19" NP671644.RAq8R_JUJRlChnkImNX8laCmOLdlNQIjIKWxk1NxFVO50130_provenance.