Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion description "[Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheochromocytoma-associated syndromes that would otherwise be missed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion evidence source_evidence_literature NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion SIO_000772 12000816 NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion wasDerivedFrom gad-20130706 NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_assertion wasGeneratedBy ECO_0000203 NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP52082.RAqUpSq1NZx452NgyJ02GP1j72b8R847fOUYE2KSucIb8130_provenance.