Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_assertion description "[The frequency of FVL was significantly greater in cancer patients with VTE compared with group 2 patients (p FVII gene, the distributions of genotypes and allele frequencies were not significantly different between two groups of patients ( p > 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_assertion evidence source_evidence_literature NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_assertion SIO_000772 20332763 NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_assertion wasDerivedFrom befree-2016 NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_assertion wasGeneratedBy ECO_0000203 NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.
- befree-2016 importedOn "2016-02-19" NP802098.RAxdVR6PhdHqVf2rRCzl9xodGCwrLo2vD9RFvxP9Mvx8s130_provenance.