Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion wasGeneratedBy ECO_0000203 NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion wasDerivedFrom gad-20150221 NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion SIO_000772 14604959 NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion evidence source_evidence_literature NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.