Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_assertion description "[The mutation screening of PTPN22 in AD patients (n=332) and controls (n=112) revealed eight missense variants, five of which have not been reported previously.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_assertion evidence source_evidence_literature NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_assertion SIO_000772 18301444 NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_assertion wasDerivedFrom befree-20150227 NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_assertion wasGeneratedBy ECO_0000203 NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP882176.RARfFB0pqmbRnRWt3klNiTKqyOukGnpebDfkbHN6IGsEM130_provenance.