Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_assertion description "[After adjustment for AF risk factors, we found significant differences in the global AGT gene haplotype profile (the global score statistic = 30.364, p = 0.001) and individual haplotype frequencies between AF patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_assertion evidence source_evidence_literature NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_assertion SIO_000772 18239384 NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_assertion wasDerivedFrom befree-20140225 NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_assertion wasGeneratedBy ECO_0000203 NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP930841.RArcXMe7b5qTSZPqEUFITMoQsOmvjqdiD7QNmuNfDvhYk130_provenance.