Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_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." NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_assertion evidence source_evidence_literature NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_assertion SIO_000772 22464776 NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_assertion wasDerivedFrom befree-20150227 NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_assertion wasGeneratedBy ECO_0000203 NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.
- befree-20150227 importedOn "2015-02-27" NP349126.RAotaKXuar0R1isYrH971JODXuwaktvY9N26eyFxWbf64130_provenance.