Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_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." NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_assertion evidence source_evidence_literature NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_assertion SIO_000772 21262951 NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_assertion wasDerivedFrom befree-20140225 NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_assertion wasGeneratedBy ECO_0000203 NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP557410.RAECknFJ6w9UwShvfTxlnUKVoxGrFrEZ_BVZE2R6gaiyM130_provenance.