Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_assertion description "[The question of whether cancer risk is associated with rare minisatellite HRAS1 alleles needs to be revisited with the use of new methods that have a greater ability to distinguish rare alleles from similarly sized common alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_assertion evidence source_evidence_literature NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_assertion SIO_000772 10601382 NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_assertion wasDerivedFrom befree-20150227 NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_assertion wasGeneratedBy ECO_0000203 NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788944.RA5aT0Prqh1RkWH1hNcbFcIJrBkFMsQQZnzOe6wVt9MLQ130_provenance.