Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_assertion description "[Specific polymorphisms in the IL4R 503, TNF (-308), and ADRB2 27 genes were independently associated with stroke susceptibility in the LV stroke subgroup, while variants in the VCAM1 (-1594) and LDLR NcoI genes were associated with SV stroke risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_assertion evidence source_evidence_literature NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_assertion SIO_000772 14615367 NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_assertion wasDerivedFrom befree-20150227 NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_assertion wasGeneratedBy ECO_0000203 NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.
- befree-20150227 importedOn "2015-02-27" NP226979.RAo4JL4oX9_0bs6jUHu0m3DFz0ydDq7U63sdJ2nF97Uac130_provenance.