Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_assertion description "[The HF pharmacogenetic literature is still in its very early stages, but there are promising candidate genetic variants that may identify which HF patients are most likely to benefit from beta-blockers and ACE inhibitors and patients that may require additional therapies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_assertion evidence source_evidence_literature NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_assertion SIO_000772 22464776 NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_assertion wasDerivedFrom befree-2016 NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_assertion wasGeneratedBy ECO_0000203 NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.
- befree-2016 importedOn "2016-02-19" NP971618.RAGIuZmnlmLILW8wEKBTNgBQOzJaGpvnSpBj8xnJB1_PA130_provenance.