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- source_evidence_literature type ECO_0000212 NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_assertion description "[Despite these figures, the screening of phaeochromocytomas and paragangliomas for mutations in the SDH genes to detect phaeochromocytoma-paraganglioma syndrome is rarely done because of time and financial constraints.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_assertion evidence source_evidence_literature NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_assertion SIO_000772 19576851 NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_assertion wasDerivedFrom befree-2016 NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_assertion wasGeneratedBy ECO_0000203 NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.
- befree-2016 importedOn "2016-02-19" NP749164.RAanx6Ibf1ZCVIOAISvvDLW2w8bj5NcJbpADJfHypTgAM130_provenance.