Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_assertion description "[Frequencies of the GG genotype and the G allele in AHSG (rs4918) were significantly higher in patients with ischemic stroke or atherosclerotic cerebral infarction than those in the control group (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_assertion evidence source_evidence_literature NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_assertion SIO_000772 23907641 NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_assertion wasDerivedFrom befree-20140225 NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_assertion wasGeneratedBy ECO_0000203 NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP527141.RAevcnNf9ZGIgja94WxOvVsQDQbaYOn0uj3xLwaxoB0XE130_provenance.