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- source_evidence_literature type ECO_0000212 NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_assertion description "[Up to 30% of pheochromocytomas and paragangliomas are associated with germline RET, Von Hippel-Lindau (VHL), neurofibromatosis type I (NF1), and succinate dehydrogenase subunits (SDHB, SDHC, and SDHD) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_assertion evidence source_evidence_literature NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_assertion SIO_000772 20236688 NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_assertion wasDerivedFrom befree-2016 NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_assertion wasGeneratedBy ECO_0000203 NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.
- befree-2016 importedOn "2016-02-19" NP800574.RAtReqEET4TbJsw-4OlMzkKrZAycVMzoSc6Ao9y7g1Fyk130_provenance.