Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_assertion description "[Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_assertion evidence source_evidence_literature NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_assertion SIO_000772 20594303 NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_assertion wasDerivedFrom befree-2016 NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_assertion wasGeneratedBy ECO_0000203 NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP822898.RAIHWUfrUsfF2CqzzHcxTq7_YTPMH3I2Z5qCuHUrVsRPQ130_provenance.