Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_assertion description "[Factor V Leiden variant was found in 1% of APS patients, in 3% of healthy individuals (p=0.49), and 16% of patients with first DVT (p<0.0005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_assertion evidence source_evidence_literature NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_assertion SIO_000772 24093662 NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_assertion wasDerivedFrom befree-20150227 NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_assertion wasGeneratedBy ECO_0000203 NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP391573.RAKmCNUNl9K59CQYi0ieNv-LkRz4xyx7CzM8JMZAYV2MU130_provenance.