Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_assertion description "[PLCE1 mutation is the most common cause of IDMS in this cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_assertion evidence source_evidence_literature NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_assertion SIO_000772 18065803 NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_assertion wasDerivedFrom befree-20140225 NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_assertion wasGeneratedBy ECO_0000203 NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488874.RAQNEoR8U7FEwrkfLk6B91lMXwbDdzumOVn072vsD2RyY130_provenance.