Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_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." NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_assertion evidence source_evidence_literature NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_assertion SIO_000772 14615367 NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_assertion wasDerivedFrom gad-20150221 NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_assertion wasGeneratedBy ECO_0000203 NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82516.RAety9dSIa4YRvkC0AtwS9UTrA_hDVDz6Ti56TdmLH80s130_provenance.