Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_assertion description "[Comparing the proportion of patients with ADAMTS13 activity below the 10th percentile within the different stroke subtypes (undetermined, cardioembolic, steno-occlusive arteriopathies), no statistically significant differences were found (undetermined, 16 of 89; cardioembolic, 6 of 40; steno-occlusive arteriopathies, 24 of 79; p = 0.08).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_assertion evidence source_evidence_literature NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_assertion SIO_000772 23225307 NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_assertion wasDerivedFrom befree-20140225 NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_assertion wasGeneratedBy ECO_0000203 NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP414344.RACt1FbhUV9HX2Dx8XOrVZl1qcO_T-22J7JWctvp5vUHQ130_provenance.