Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_assertion description "[Patients with NF1 and MEN 2 could be discriminated from those with VHL, SDHB, and SDHD gene mutations in 99% of cases by the combination of normetanephrine and metanephrine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_assertion evidence source_evidence_literature NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_assertion SIO_000772 21262951 NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_assertion wasDerivedFrom befree-20140225 NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_assertion wasGeneratedBy ECO_0000203 NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209571.RAWVfbTz6-fEM8OyTp2e_Z2hWPjC04J18YdELQ6-Tljxo130_provenance.