Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_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." NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_assertion evidence source_evidence_literature NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_assertion SIO_000772 10601382 NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_assertion wasDerivedFrom befree-20140225 NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_assertion wasGeneratedBy ECO_0000203 NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP609186.RA9lxXlh9ePwchE5mvcLD7-AYxTIiow_VPGgb8mDYgMEM130_provenance.