Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_assertion description "[ None of these 120 patients consulting for unexplained chronic fatigue was found with hereditary haemochromatosis. Therefore observed prevalence is 0, with upper limit of 95% confidence interval at 2.5%. But the high prevalence (38%) of serum ferritin >or]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_assertion evidence source_evidence_literature NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_assertion SIO_000772 15363617 NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_assertion wasDerivedFrom gad-20150221 NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_assertion wasGeneratedBy ECO_0000203 NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP50143.RAXBCFAG9RIr7az9TP4Qhm6JTqmYN92mVhZdH8iQGDJWA130_provenance.