Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_assertion description "[The frequency of PRSS1 mutation was present in 21.4% of ICP patients, which was significantly higher (p < 0.05) than in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_assertion evidence source_evidence_literature NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_assertion SIO_000772 20676769 NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_assertion wasDerivedFrom befree-20150227 NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_assertion wasGeneratedBy ECO_0000203 NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP649500.RAgl6BF7a7d0r7PkUi2momRKNR5wVc5TuB4kBPs-Enpp8130_provenance.