Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_assertion description "[No significant differences in the frequency of the G-455, 353Q or 4G alleles, or in the genotype distribution for beta-fibrinogen, factor VII and PAI-1 were observed between patients with IHD and those without IHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_assertion evidence source_evidence_literature NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_assertion SIO_000772 12141403 NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_assertion wasDerivedFrom befree-2016 NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_assertion wasGeneratedBy ECO_0000203 NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP362596.RAe3N8b84FfWzcFYWLXoKQcoAb5cWDi-HBz7mq3vGVjWU130_provenance.