Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_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." NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_assertion evidence source_evidence_literature NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_assertion SIO_000772 19414860 NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_assertion wasDerivedFrom befree-20150227 NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_assertion wasGeneratedBy ECO_0000203 NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP281910.RAa4rJzLJ3XvUQ8rmlt9nPeymY2BvJmsiToSptvilOvcQ130_provenance.