Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_assertion description "[It is noteworthy that genetic variants in CASP8 were associated with risk of all major NHL subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_assertion evidence source_evidence_literature NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_assertion SIO_000772 19414860 NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_assertion wasDerivedFrom befree-20140225 NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_assertion wasGeneratedBy ECO_0000203 NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806397.RAW2ZbT3Ci3lXJJ0jmyLam53i83ALhStg49exgS6x-k-s130_provenance.