Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_assertion description "[Genotypes for VEGFA polymorphisms can be useful to help to identify hypertensive patients at greater intrinsic risk for heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_assertion evidence source_evidence_literature NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_assertion SIO_000772 24321896 NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_assertion wasDerivedFrom befree-2016 NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_assertion wasGeneratedBy ECO_0000203 NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1135199.RAlXsvozO1szIdV861rLAIjpet4Rm3BAUc7D7OCF2VWwE130_provenance.