Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_assertion description "[The frequency of 213PP genotype and P allele of the L-selectin gene in patients with T2D was significantly higher than that in controls (P=0.007; P=0.019, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_assertion evidence source_evidence_literature NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_assertion SIO_000772 22921892 NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_assertion wasDerivedFrom befree-20140225 NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_assertion wasGeneratedBy ECO_0000203 NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP571047.RAXgjGYHxcv7k_X2bm0BXcWWLOQiDsLT_JyjFhzB11S9g130_provenance.