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- source_evidence_literature type ECO_0000212 NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_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." NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_assertion evidence source_evidence_literature NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_assertion SIO_000772 21262951 NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_assertion wasDerivedFrom befree-2016 NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_assertion wasGeneratedBy ECO_0000203 NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.
- befree-2016 importedOn "2016-02-19" NP867361.RAc6Umk0mXo6m2QZlJNxG_G65znmUyS-NAJpP4JpdnaOE130_provenance.