Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion> ?p ?o ?g. }
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- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion type Assertion NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_head.
- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion description "[Evaluation of genetic variation for E-selectin L554F polymorphisms revealed that the frequency of minor allele (F) and its heterozygous genotype (LF) is almost 4 times higher in the stroke patients than the controls (16.7 vs. 4.3 and 33.4 vs. 8.5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion evidence source_evidence_literature NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion SIO_000772 19420919 NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion wasDerivedFrom gad-20150221 NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_assertion wasGeneratedBy ECO_0000203 NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.