Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_assertion description "[In Caucasians, we found significant within-family association results between the COL1A1-Sp1 polymorphism (rs1800012) and cross sectional area (CSA), cortical thickness (CT), endocortical diameter (ED), buckling ratio (BR) (P=0.018, 0.002, 0.023, and 0.001, respectively); the COL1A1-Sp1 polymorphism also detected significant linkage with BR (P=0.039).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_assertion evidence source_evidence_literature NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_assertion SIO_000772 17303000 NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_assertion wasDerivedFrom befree-20140225 NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_assertion wasGeneratedBy ECO_0000203 NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551211.RAQJRKKqQJ76USLdbxxs8LnEA2YQ8Vy-TWqLlqmWmimCc130_provenance.