Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_assertion description "[insertion/deletion (I/D) is one of angiotensin I converting enzyme (ACE) polymorphisms and A1166C is one of angiotensin II type-1 receptor (AT1R) polymorphisms which have been associated with various diseases such as cardiovascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_assertion evidence source_evidence_literature NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_assertion SIO_000772 20945417 NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_assertion wasDerivedFrom befree-2016 NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_assertion wasGeneratedBy ECO_0000203 NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.
- befree-2016 importedOn "2016-02-19" NP845552.RAGqF2IludGfiKg6wbWOQIFmJWiA1SxEZjMhrLkAsVYeA130_provenance.