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- source_evidence_literature type ECO_0000212 NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_assertion description "[Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_assertion evidence source_evidence_literature NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_assertion SIO_000772 12142464 NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_assertion wasDerivedFrom befree-20150227 NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_assertion wasGeneratedBy ECO_0000203 NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.
- befree-20150227 importedOn "2015-02-27" NP802251.RAVFOVeYx8bN74xyQJLmDrTL53FG4eqYkL4nQrnD3uvso130_provenance.