Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP146712.RA2im6jTDQUDGa0h7CbuT5tytZbdgthVruO324DrCVFmE130_provenance.