Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_assertion description "[Deletion of the PMP22 gene, results in hereditary neuropathy with liability to pressure palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_assertion evidence source_evidence_literature NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_assertion SIO_000772 25720245 NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_assertion wasDerivedFrom befree-2016 NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_assertion wasGeneratedBy ECO_0000203 NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266485.RAib8umgKG4jchDFYk4M1gls3xZ6YevrJ68gHWyxIIbZE130_provenance.