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- source_evidence_literature type ECO_0000212 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion description "[Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion evidence source_evidence_literature NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion SIO_000772 16717225 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion wasDerivedFrom befree-20150227 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_assertion wasGeneratedBy ECO_0000203 NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.
- befree-20150227 importedOn "2015-02-27" NP227599.RA4px8H9YZN48IRDCy8XYLqPVaVYeTRGMiq-Hs5XvmVek130_provenance.